6-135516875-CCCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516875
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516871
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.940-6_940-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1282_948+1285delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+152_103+155delAAGG
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*538-6_*538-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1065-6_1065-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*416-6_*416-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.940-6_940-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.940-6_940-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.949-6_949-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.940-6_940-3delCCTT
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.949-6_949-3delCCTT
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: CCCTT
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

6-135516876-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516876
    reference: chr 6
allele count: 7
allele frequency: 5.768533473975673e-5
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.940-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1278C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*18-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1278C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.844-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.940-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.949-10C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.940-10C>G
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

6-135516879-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516879
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516879
    reference: chr 6
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.940-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.940-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*18-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*18-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.940-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*538-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*18-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*18-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.949-7T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.844-7T>G
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.949-7T>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

6-135516886-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516886
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516886
    reference: chr 6
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*18A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.1A>T
  hgvsp: ENSP00000432042.1:p.Thr1?
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.949A>T
  hgvsp: ENSP00000433227.1:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.949A>T
  hgvsp: ENSP00000356788.4:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.949A>T
  hgvsp: ENSP00000413011.2:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+145T>A
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.949A>T
  hgvsp: ENSP00000434917.1:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.949A>T
  hgvsp: ENSP00000356786.2:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*18A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1288A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.940A>T
  hgvsp: ENSP00000433844.1:p.Thr314Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.949A>T
  hgvsp: ENSP00000432811.1:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.949A>T
  hgvsp: ENSP00000432168.1:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.949A>T
  hgvsp: ENSP00000434420.1:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.949A>T
  hgvsp: ENSP00000432948.1:p.Thr317Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.844A>T
  hgvsp: ENSP00000436605.1:p.Thr282Ser
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.940A>T
  hgvsp: ENSP00000434723.1:p.Thr314Ser
  variant of: http://identifiers.org/hgnc/7545
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr1?
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-135516902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516902
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516902
    reference: chr 6
allele count: 10
allele frequency: 8.237232289950576e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1304G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*432G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.965G>A
  hgvsp: ENSP00000434420.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.956G>A
  hgvsp: ENSP00000433458.1:p.Cys319Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.965G>A
  hgvsp: ENSP00000432948.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.965G>A
  hgvsp: ENSP00000435055.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.965G>A
  hgvsp: ENSP00000432851.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.965G>A
  hgvsp: ENSP00000339992.5:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.17G>A
  hgvsp: ENSP00000432042.1:p.Cys6Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.860G>A
  hgvsp: ENSP00000436605.1:p.Cys287Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.965G>A
  hgvsp: ENSP00000434917.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.965G>A
  hgvsp: ENSP00000435293.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.956G>A
  hgvsp: ENSP00000434795.1:p.Cys319Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.965G>A
  hgvsp: ENSP00000326328.8:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.965G>A
  hgvsp: ENSP00000433227.1:p.Cys322Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.956G>A
  hgvsp: ENSP00000433844.1:p.Cys319Tyr
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys322Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

6-135516907-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516907
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516907
    reference: chr 6
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*559T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.970T>G
  hgvsp: ENSP00000434639.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.961T>G
  hgvsp: ENSP00000410825.2:p.Tyr321Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.970T>G
  hgvsp: ENSP00000413011.2:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.970T>G
  hgvsp: ENSP00000341050.5:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.970T>G
  hgvsp: ENSP00000432168.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1309T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.970T>G
  hgvsp: ENSP00000339992.5:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.961T>G
  hgvsp: ENSP00000433844.1:p.Tyr321Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*39T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.970T>G
  hgvsp: ENSP00000326328.8:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.970T>G
  hgvsp: ENSP00000435293.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.961T>G
  hgvsp: ENSP00000433458.1:p.Tyr321Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*39T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.970T>G
  hgvsp: ENSP00000434420.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.970T>G
  hgvsp: ENSP00000432851.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.970T>G
  hgvsp: ENSP00000432811.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.970T>G
  hgvsp: ENSP00000434816.1:p.Tyr324Asp
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr324Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/6-135516911-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516911
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516911
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.974C>A
  hgvsp: ENSP00000435293.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.974C>A
  hgvsp: ENSP00000434917.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.974C>A
  hgvsp: ENSP00000432948.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.974C>A
  hgvsp: ENSP00000432811.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.974C>A
  hgvsp: ENSP00000432851.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.974C>A
  hgvsp: ENSP00000433745.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.974C>A
  hgvsp: ENSP00000356786.2:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.974C>A
  hgvsp: ENSP00000341050.5:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.974C>A
  hgvsp: ENSP00000432168.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.974C>A
  hgvsp: ENSP00000435055.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*43C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.974C>A
  hgvsp: ENSP00000339992.5:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1090C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.965C>A
  hgvsp: ENSP00000410825.2:p.Pro322His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.974C>A
  hgvsp: ENSP00000434816.1:p.Pro325His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.965C>A
  hgvsp: ENSP00000434795.1:p.Pro322His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.869C>A
  hgvsp: ENSP00000436605.1:p.Pro290His
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+120G>T
  variant of: http://identifiers.org/hgnc/37457
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro325His
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

6-135516912-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516912
    reference: chr 6
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.975C>G
  hgvsp: ENST00000339290.5:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.966C>G
  hgvsp: ENST00000526889.1:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.975C>G
  hgvsp: ENST00000534044.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.975C>G
  hgvsp: ENST00000533384.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.975C>G
  hgvsp: ENST00000367814.4:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.966C>G
  hgvsp: ENST00000528774.1:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.870C>G
  hgvsp: ENST00000533624.1:c.870C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.975C>G
  hgvsp: ENST00000533837.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.975C>G
  hgvsp: ENST00000528140.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.975C>G
  hgvsp: ENST00000534121.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+119G>C
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.975C>G
  hgvsp: ENST00000528015.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.975C>G
  hgvsp: ENST00000438901.2:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.975C>G
  hgvsp: ENST00000531737.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.975C>G
  hgvsp: ENST00000527615.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.975C>G
  hgvsp: ENST00000525002.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.975C>G
  hgvsp: ENST00000533808.1:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.966C>G
  hgvsp: ENST00000442647.2:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro325Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

6-135516912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516912
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.975C>T
  hgvsp: ENST00000528015.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.870C>T
  hgvsp: ENST00000533624.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.975C>T
  hgvsp: ENST00000533837.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.975C>T
  hgvsp: ENST00000525940.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.975C>T
  hgvsp: ENST00000367814.4:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.975C>T
  hgvsp: ENST00000367812.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.975C>T
  hgvsp: ENST00000438901.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.975C>T
  hgvsp: ENST00000341911.5:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*44C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.966C>T
  hgvsp: ENST00000526187.1:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.975C>T
  hgvsp: ENST00000528140.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.975C>T
  hgvsp: ENST00000534121.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.975C>T
  hgvsp: ENST00000316528.8:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.975C>T
  hgvsp: ENST00000533808.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.975C>T
  hgvsp: ENST00000525002.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.975C>T
  hgvsp: ENST00000534044.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.975C>T
  hgvsp: ENST00000526320.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.975C>T
  hgvsp: ENST00000531737.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro325Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-135516913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516913
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516913
    reference: chr 6
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*45G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.871G>A
  hgvsp: ENSP00000436605.1:p.Gly291Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*45G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.976G>A
  hgvsp: ENSP00000326328.8:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.976G>A
  hgvsp: ENSP00000433227.1:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.967G>A
  hgvsp: ENSP00000434795.1:p.Gly323Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.976G>A
  hgvsp: ENSP00000432811.1:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*45G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.976G>A
  hgvsp: ENSP00000432877.1:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.976G>A
  hgvsp: ENSP00000341050.5:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.976G>A
  hgvsp: ENSP00000433745.1:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.967G>A
  hgvsp: ENSP00000433458.1:p.Gly323Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.976G>A
  hgvsp: ENSP00000339992.5:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.976G>A
  hgvsp: ENSP00000413011.2:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*565G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.976G>A
  hgvsp: ENSP00000434917.1:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.976G>A
  hgvsp: ENSP00000432948.1:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.976G>A
  hgvsp: ENSP00000356786.2:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly326Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

6-135516923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516923
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516923
    reference: chr 6
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.986G>A
  hgvsp: ENSP00000356788.4:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.986G>A
  hgvsp: ENSP00000326328.8:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*55G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.986G>A
  hgvsp: ENSP00000434816.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*575G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.986G>A
  hgvsp: ENSP00000432948.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1102G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*55G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.986G>A
  hgvsp: ENSP00000434917.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.881G>A
  hgvsp: ENSP00000436605.1:p.Ser294Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.986G>A
  hgvsp: ENSP00000432168.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.986G>A
  hgvsp: ENSP00000434639.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.986G>A
  hgvsp: ENSP00000432877.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.977G>A
  hgvsp: ENSP00000433458.1:p.Ser326Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.986G>A
  hgvsp: ENSP00000339992.5:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.986G>A
  hgvsp: ENSP00000432851.1:p.Ser329Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.977G>A
  hgvsp: ENSP00000433844.1:p.Ser326Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.977G>A
  hgvsp: ENSP00000434795.1:p.Ser326Asn
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser329Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

6-135516930-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516930
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516930
    reference: chr 6
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.984C>T
  hgvsp: ENST00000526889.1:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.984C>T
  hgvsp: ENST00000529262.1:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.993C>T
  hgvsp: ENST00000533837.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.993C>T
  hgvsp: ENST00000528140.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.993C>T
  hgvsp: ENST00000341911.5:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.993C>T
  hgvsp: ENST00000527615.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.993C>T
  hgvsp: ENST00000534121.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.993C>T
  hgvsp: ENST00000533384.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.984C>T
  hgvsp: ENST00000526187.1:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.993C>T
  hgvsp: ENST00000528343.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.45C>T
  hgvsp: ENST00000534736.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.993C>T
  hgvsp: ENST00000533808.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.993C>T
  hgvsp: ENST00000525940.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.993C>T
  hgvsp: ENST00000534044.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.993C>T
  hgvsp: ENST00000528015.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.888C>T
  hgvsp: ENST00000533624.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1332C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.993C>T
  hgvsp: ENST00000526320.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr331Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum

6-135516936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516936
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516936
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*68C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.990C>T
  hgvsp: ENST00000529262.1:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.990C>T
  hgvsp: ENST00000528774.1:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.999C>T
  hgvsp: ENST00000531737.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.999C>T
  hgvsp: ENST00000528140.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.999C>T
  hgvsp: ENST00000526320.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.999C>T
  hgvsp: ENST00000528015.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.999C>T
  hgvsp: ENST00000367814.4:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*68C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1338C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.999C>T
  hgvsp: ENST00000533837.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.894C>T
  hgvsp: ENST00000533624.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.999C>T
  hgvsp: ENST00000534044.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.999C>T
  hgvsp: ENST00000533808.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.999C>T
  hgvsp: ENST00000339290.5:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.999C>T
  hgvsp: ENST00000533384.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.999C>T
  hgvsp: ENST00000525002.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.999C>T
  hgvsp: ENST00000534121.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala333Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ

6-135516937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516937
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516937
    reference: chr 6
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1000G>A
  hgvsp: ENSP00000326328.8:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*69G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1000G>A
  hgvsp: ENSP00000434420.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1000G>A
  hgvsp: ENSP00000356788.4:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1000G>A
  hgvsp: ENSP00000435293.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1000G>A
  hgvsp: ENSP00000434639.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.991G>A
  hgvsp: ENSP00000434795.1:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1000G>A
  hgvsp: ENSP00000432948.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.895G>A
  hgvsp: ENSP00000436605.1:p.Asp299Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*69G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.991G>A
  hgvsp: ENSP00000433844.1:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1000G>A
  hgvsp: ENSP00000432877.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.991G>A
  hgvsp: ENSP00000410825.2:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1000G>A
  hgvsp: ENSP00000434917.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*467G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.991G>A
  hgvsp: ENSP00000434723.1:p.Asp331Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1000G>A
  hgvsp: ENSP00000435055.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1339G>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp334Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

6-135516940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516940
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516940
    reference: chr 6
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1119C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*72C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1003C>T
  hgvsp: ENSP00000434639.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1003C>T
  hgvsp: ENSP00000435055.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1003C>T
  hgvsp: ENSP00000432811.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1003C>T
  hgvsp: ENSP00000434917.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+91G>A
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1003C>T
  hgvsp: ENSP00000326328.8:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*72C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1003C>T
  hgvsp: ENSP00000341050.5:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1003C>T
  hgvsp: ENSP00000434420.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1003C>T
  hgvsp: ENSP00000435293.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.994C>T
  hgvsp: ENSP00000434723.1:p.His332Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*470C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1003C>T
  hgvsp: ENSP00000432877.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1003C>T
  hgvsp: ENSP00000356786.2:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1003C>T
  hgvsp: ENSP00000433745.1:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1003C>T
  hgvsp: ENSP00000339992.5:p.His335Tyr
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His335Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

6-135516942-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516942
    reference: chr 6
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1005C>G
  hgvsp: ENSP00000432948.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*74C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1005C>G
  hgvsp: ENSP00000413011.2:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1005C>G
  hgvsp: ENSP00000434816.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1005C>G
  hgvsp: ENSP00000434917.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1005C>G
  hgvsp: ENSP00000435055.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1005C>G
  hgvsp: ENSP00000326328.8:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1005C>G
  hgvsp: ENSP00000341050.5:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1005C>G
  hgvsp: ENSP00000434639.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.996C>G
  hgvsp: ENSP00000433458.1:p.His332Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1005C>G
  hgvsp: ENSP00000432877.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*74C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1005C>G
  hgvsp: ENSP00000339992.5:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*74C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1005C>G
  hgvsp: ENSP00000435293.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.996C>G
  hgvsp: ENSP00000410825.2:p.His332Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1005C>G
  hgvsp: ENSP00000432851.1:p.His335Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1121C>G
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His335Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

6-135516944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516944
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516944
    reference: chr 6
allele count: 124
allele frequency: 1.02136632456386e-3
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.902C>T
  hgvsp: ENSP00000436605.1:p.Thr301Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.998C>T
  hgvsp: ENSP00000410825.2:p.Thr333Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1007C>T
  hgvsp: ENSP00000432948.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.998C>T
  hgvsp: ENSP00000434795.1:p.Thr333Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1007C>T
  hgvsp: ENSP00000434639.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1346C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1007C>T
  hgvsp: ENSP00000435055.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1007C>T
  hgvsp: ENSP00000434816.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1007C>T
  hgvsp: ENSP00000432168.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1123C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1007C>T
  hgvsp: ENSP00000433227.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1007C>T
  hgvsp: ENSP00000326328.8:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*474C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*596C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1007C>T
  hgvsp: ENSP00000339992.5:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1007C>T
  hgvsp: ENSP00000432851.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1007C>T
  hgvsp: ENSP00000432811.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1007C>T
  hgvsp: ENSP00000356788.4:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*76C>T
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr336Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

6-135516945-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516945
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516945
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.60C>G
  hgvsp: ENST00000534736.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.999C>G
  hgvsp: ENST00000528774.1:c.999C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1008C>G
  hgvsp: ENST00000533384.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1008C>G
  hgvsp: ENST00000527615.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1008C>G
  hgvsp: ENST00000367812.2:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1008C>G
  hgvsp: ENST00000533837.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1008C>G
  hgvsp: ENST00000528343.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1347C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1008C>G
  hgvsp: ENST00000528140.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1008C>G
  hgvsp: ENST00000534044.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1008C>G
  hgvsp: ENST00000528015.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1008C>G
  hgvsp: ENST00000531737.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*77C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1008C>G
  hgvsp: ENST00000534121.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1008C>G
  hgvsp: ENST00000438901.2:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1008C>G
  hgvsp: ENST00000533808.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*77C>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1008C>G
  hgvsp: ENST00000526320.1:c.1008C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr336Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

6-135516945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516945
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516945
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.999C>T
  hgvsp: ENST00000529262.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1008C>T
  hgvsp: ENST00000527615.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1008C>T
  hgvsp: ENST00000533384.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1008C>T
  hgvsp: ENST00000533808.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1008C>T
  hgvsp: ENST00000526320.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1347C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1008C>T
  hgvsp: ENST00000367814.4:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1008C>T
  hgvsp: ENST00000316528.8:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1008C>T
  hgvsp: ENST00000528140.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.999C>T
  hgvsp: ENST00000442647.2:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*77C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.999C>T
  hgvsp: ENST00000526187.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1008C>T
  hgvsp: ENST00000534121.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1008C>T
  hgvsp: ENST00000528015.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1008C>T
  hgvsp: ENST00000528343.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1008C>T
  hgvsp: ENST00000525940.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1008C>T
  hgvsp: ENST00000533837.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*77C>T
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr336Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-135516946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516946
    reference: chr 6
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1000A>G
  hgvsp: ENSP00000410825.2:p.Arg334Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1009A>G
  hgvsp: ENSP00000434420.1:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1348A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1009A>G
  hgvsp: ENSP00000356786.2:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1009A>G
  hgvsp: ENSP00000339992.5:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1348A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*476A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*78A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1000A>G
  hgvsp: ENSP00000434795.1:p.Arg334Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1009A>G
  hgvsp: ENSP00000356788.4:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1009A>G
  hgvsp: ENSP00000434639.1:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+85T>C
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1009A>G
  hgvsp: ENSP00000434816.1:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1009A>G
  hgvsp: ENSP00000432851.1:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1125A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1009A>G
  hgvsp: ENSP00000341050.5:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*78A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1009A>G
  hgvsp: ENSP00000435055.1:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1009A>G
  hgvsp: ENSP00000432877.1:p.Arg337Gly
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg337Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

6-135516954-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516954
    reference: chr 6
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.69T>G
  hgvsp: ENSP00000432042.1:p.His23Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1017T>G
  hgvsp: ENSP00000356788.4:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1017T>G
  hgvsp: ENSP00000432948.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1017T>G
  hgvsp: ENSP00000435055.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1008T>G
  hgvsp: ENSP00000434795.1:p.His336Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1017T>G
  hgvsp: ENSP00000326328.8:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1017T>G
  hgvsp: ENSP00000434816.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1017T>G
  hgvsp: ENSP00000432811.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.912T>G
  hgvsp: ENSP00000436605.1:p.His304Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1017T>G
  hgvsp: ENSP00000413011.2:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1017T>G
  hgvsp: ENSP00000339992.5:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*86T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1017T>G
  hgvsp: ENSP00000434917.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1017T>G
  hgvsp: ENSP00000433745.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1356T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1008T>G
  hgvsp: ENSP00000433458.1:p.His336Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1017T>G
  hgvsp: ENSP00000434639.1:p.His339Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1008T>G
  hgvsp: ENSP00000434723.1:p.His336Gln
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His339Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

6-135516974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516974
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516974
    reference: chr 6
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1037C>T
  hgvsp: ENSP00000434639.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1037C>T
  hgvsp: ENSP00000435293.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1037C>T
  hgvsp: ENSP00000432811.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1028C>T
  hgvsp: ENSP00000434795.1:p.Ser343Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1037C>T
  hgvsp: ENSP00000356788.4:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1037C>T
  hgvsp: ENSP00000433227.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1037C>T
  hgvsp: ENSP00000434917.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1037C>T
  hgvsp: ENSP00000432877.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1037C>T
  hgvsp: ENSP00000356786.2:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1037C>T
  hgvsp: ENSP00000326328.8:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1037C>T
  hgvsp: ENSP00000341050.5:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.932C>T
  hgvsp: ENSP00000436605.1:p.Ser311Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1037C>T
  hgvsp: ENSP00000434420.1:p.Ser346Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1028C>T
  hgvsp: ENSP00000433458.1:p.Ser343Phe
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser346Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

6-135516983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516983
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516983
    reference: chr 6
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+48C>T
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1046G>A
  hgvsp: ENSP00000434917.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1046G>A
  hgvsp: ENSP00000435293.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1046G>A
  hgvsp: ENSP00000435055.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.941G>A
  hgvsp: ENSP00000436605.1:p.Gly314Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1046G>A
  hgvsp: ENSP00000432877.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1046G>A
  hgvsp: ENSP00000356788.4:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1046G>A
  hgvsp: ENSP00000339992.5:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1037G>A
  hgvsp: ENSP00000433458.1:p.Gly346Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*115G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1046G>A
  hgvsp: ENSP00000433227.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1046G>A
  hgvsp: ENSP00000434420.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1046G>A
  hgvsp: ENSP00000413011.2:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1046G>A
  hgvsp: ENSP00000326328.8:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1046G>A
  hgvsp: ENSP00000432168.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1046G>A
  hgvsp: ENSP00000433745.1:p.Gly349Glu
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly349Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

6-135516986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516986
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516986
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1049A>G
  hgvsp: ENSP00000339992.5:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.944A>G
  hgvsp: ENSP00000436605.1:p.Glu315Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1049A>G
  hgvsp: ENSP00000432877.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*516A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1049A>G
  hgvsp: ENSP00000432948.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1049A>G
  hgvsp: ENSP00000356788.4:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*118A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1049A>G
  hgvsp: ENSP00000434639.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1040A>G
  hgvsp: ENSP00000410825.2:p.Glu347Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1049A>G
  hgvsp: ENSP00000432168.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1049A>G
  hgvsp: ENSP00000435293.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1049A>G
  hgvsp: ENSP00000433227.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1049A>G
  hgvsp: ENSP00000432851.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1049A>G
  hgvsp: ENSP00000432811.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1049A>G
  hgvsp: ENSP00000326328.8:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.101A>G
  hgvsp: ENSP00000432042.1:p.Glu34Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1049A>G
  hgvsp: ENSP00000434917.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1049A>G
  hgvsp: ENSP00000434816.1:p.Glu350Gly
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu350Gly
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-135516988-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516988
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516988
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1051C>A
  hgvsp: ENSP00000435293.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1042C>A
  hgvsp: ENSP00000433844.1:p.His348Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1051C>A
  hgvsp: ENSP00000434639.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.103C>A
  hgvsp: ENSP00000432042.1:p.His35Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.946C>A
  hgvsp: ENSP00000436605.1:p.His316Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1051C>A
  hgvsp: ENSP00000326328.8:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*120C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1051C>A
  hgvsp: ENSP00000434816.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1051C>A
  hgvsp: ENSP00000432811.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1051C>A
  hgvsp: ENSP00000435055.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1051C>A
  hgvsp: ENSP00000432168.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1051C>A
  hgvsp: ENSP00000339992.5:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1051C>A
  hgvsp: ENSP00000434420.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1051C>A
  hgvsp: ENSP00000341050.5:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1051C>A
  hgvsp: ENSP00000432948.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1051C>A
  hgvsp: ENSP00000434917.1:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1051C>A
  hgvsp: ENSP00000356786.2:p.His351Asn
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1042C>A
  hgvsp: ENSP00000434795.1:p.His348Asn
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His351Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/6-135516990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516990
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516990
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1053C>A
  hgvsp: ENSP00000434420.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*520C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1053C>A
  hgvsp: ENSP00000435055.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1053C>A
  hgvsp: ENSP00000326328.8:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1053C>A
  hgvsp: ENSP00000432948.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*122C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.105C>A
  hgvsp: ENSP00000432042.1:p.His35Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1053C>A
  hgvsp: ENSP00000339992.5:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1053C>A
  hgvsp: ENSP00000432168.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+41G>T
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*122C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1053C>A
  hgvsp: ENSP00000433227.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1053C>A
  hgvsp: ENSP00000341050.5:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1392C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1044C>A
  hgvsp: ENSP00000433458.1:p.His348Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1053C>A
  hgvsp: ENSP00000435293.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1053C>A
  hgvsp: ENSP00000434816.1:p.His351Gln
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1044C>A
  hgvsp: ENSP00000434795.1:p.His348Gln
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His351Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-135516995-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135516995
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135516995
    reference: chr 6
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1058C>A
  hgvsp: ENSP00000326328.8:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1058C>A
  hgvsp: ENSP00000356786.2:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*127C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.110C>A
  hgvsp: ENSP00000432042.1:p.Ser37Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1058C>A
  hgvsp: ENSP00000435055.1:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1058C>A
  hgvsp: ENSP00000432811.1:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1049C>A
  hgvsp: ENSP00000410825.2:p.Ser350Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1049C>A
  hgvsp: ENSP00000434723.1:p.Ser350Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1058C>A
  hgvsp: ENSP00000339992.5:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1058C>A
  hgvsp: ENSP00000432851.1:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*127C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.953C>A
  hgvsp: ENSP00000436605.1:p.Ser318Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1058C>A
  hgvsp: ENSP00000434420.1:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*127C>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1058C>A
  hgvsp: ENSP00000432877.1:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1058C>A
  hgvsp: ENSP00000434639.1:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1058C>A
  hgvsp: ENSP00000413011.2:p.Ser353Tyr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1397C>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser353Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-135517001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517001
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517001
    reference: chr 6
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1064C>T
  hgvsp: ENSP00000432851.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1064C>T
  hgvsp: ENSP00000326328.8:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1064C>T
  hgvsp: ENSP00000432948.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1064C>T
  hgvsp: ENSP00000434816.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1055C>T
  hgvsp: ENSP00000433458.1:p.Pro352Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1064C>T
  hgvsp: ENSP00000435293.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1064C>T
  hgvsp: ENSP00000434639.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1064C>T
  hgvsp: ENSP00000356786.2:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1403C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1064C>T
  hgvsp: ENSP00000339992.5:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1064C>T
  hgvsp: ENSP00000356788.4:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*133C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1064C>T
  hgvsp: ENSP00000433227.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1403C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1055C>T
  hgvsp: ENSP00000410825.2:p.Pro352Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1064C>T
  hgvsp: ENSP00000433745.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1064C>T
  hgvsp: ENSP00000434917.1:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*531C>T
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro355Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum

6-135517013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517013
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517013
    reference: chr 6
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1076C>T
  hgvsp: ENSP00000434816.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*145C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1076C>T
  hgvsp: ENSP00000432168.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1076C>T
  hgvsp: ENSP00000341050.5:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1076C>T
  hgvsp: ENSP00000434420.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1067C>T
  hgvsp: ENSP00000434723.1:p.Ala356Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1067C>T
  hgvsp: ENSP00000433844.1:p.Ala356Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1415C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1076C>T
  hgvsp: ENSP00000433227.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1076C>T
  hgvsp: ENSP00000356788.4:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1076C>T
  hgvsp: ENSP00000434917.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1076C>T
  hgvsp: ENSP00000434639.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1076C>T
  hgvsp: ENSP00000326328.8:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1076C>T
  hgvsp: ENSP00000435293.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.128C>T
  hgvsp: ENSP00000432042.1:p.Ala43Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1076C>T
  hgvsp: ENSP00000413011.2:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1076C>T
  hgvsp: ENSP00000432948.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1076C>T
  hgvsp: ENSP00000432851.1:p.Ala359Val
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala359Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

6-135517014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517014
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517014
    reference: chr 6
allele count: 31
allele frequency: 2.554425748611546e-4
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1077G>A
  hgvsp: ENST00000534044.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1077G>A
  hgvsp: ENST00000367812.2:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1077G>A
  hgvsp: ENST00000438901.2:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*146G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.972G>A
  hgvsp: ENST00000533624.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*146G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1077G>A
  hgvsp: ENST00000528015.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1068G>A
  hgvsp: ENST00000442647.2:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1077G>A
  hgvsp: ENST00000527615.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1068G>A
  hgvsp: ENST00000526889.1:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1077G>A
  hgvsp: ENST00000534121.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1068G>A
  hgvsp: ENST00000529262.1:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1077G>A
  hgvsp: ENST00000367814.4:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1077G>A
  hgvsp: ENST00000533384.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1077G>A
  hgvsp: ENST00000316528.8:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1077G>A
  hgvsp: ENST00000526320.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1068G>A
  hgvsp: ENST00000526187.1:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1193G>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala359Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

6-135517020-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517020
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517020
    reference: chr 6
allele count: 9
allele frequency: 7.415097137772504e-5
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1074T>G
  hgvsp: ENST00000529262.1:c.1074T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1074T>G
  hgvsp: ENST00000526187.1:c.1074T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1083T>G
  hgvsp: ENST00000534121.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*672T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1083T>G
  hgvsp: ENST00000341911.5:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1083T>G
  hgvsp: ENST00000527615.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*152T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1083T>G
  hgvsp: ENST00000533808.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.135T>G
  hgvsp: ENST00000534736.1:c.135T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*152T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1083T>G
  hgvsp: ENST00000531737.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1083T>G
  hgvsp: ENST00000367812.2:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1083T>G
  hgvsp: ENST00000528140.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1074T>G
  hgvsp: ENST00000526889.1:c.1074T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1083T>G
  hgvsp: ENST00000526320.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1074T>G
  hgvsp: ENST00000442647.2:c.1074T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1083T>G
  hgvsp: ENST00000533837.1:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1083T>G
  hgvsp: ENST00000367814.4:c.1083T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro361Pro
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

6-135517022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517022
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517022
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1085G>A
  hgvsp: ENSP00000339992.5:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1085G>A
  hgvsp: ENSP00000432168.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1085G>A
  hgvsp: ENSP00000432811.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1085G>A
  hgvsp: ENSP00000434917.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*552G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1085G>A
  hgvsp: ENSP00000326328.8:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1085G>A
  hgvsp: ENSP00000433227.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1424G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.103+9C>T
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*154G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1085G>A
  hgvsp: ENSP00000433745.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1085G>A
  hgvsp: ENSP00000432851.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1085G>A
  hgvsp: ENSP00000432948.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1076G>A
  hgvsp: ENSP00000433844.1:p.Gly359Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1076G>A
  hgvsp: ENSP00000434723.1:p.Gly359Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1076G>A
  hgvsp: ENSP00000433458.1:p.Gly359Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1201G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*154G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1085G>A
  hgvsp: ENSP00000435055.1:p.Gly362Asp
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly362Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-135517041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517041
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517041
    reference: chr 6
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*693C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1104C>T
  hgvsp: ENST00000528140.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1095C>T
  hgvsp: ENST00000526187.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.156C>T
  hgvsp: ENST00000534736.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.999C>T
  hgvsp: ENST00000533624.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1443C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1104C>T
  hgvsp: ENST00000534044.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1104C>T
  hgvsp: ENST00000528015.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1104C>T
  hgvsp: ENST00000533837.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1104C>T
  hgvsp: ENST00000528343.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1104C>T
  hgvsp: ENST00000341911.5:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1104C>T
  hgvsp: ENST00000533384.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1095C>T
  hgvsp: ENST00000529262.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1104C>T
  hgvsp: ENST00000526320.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.93G>A
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1095C>T
  hgvsp: ENST00000528774.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1104C>T
  hgvsp: ENST00000527615.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser368Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-135517042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517042
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517042
    reference: chr 6
allele count: 36
allele frequency: 2.966478789676654e-4
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1105G>A
  hgvsp: ENSP00000432811.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*174G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1105G>A
  hgvsp: ENSP00000434639.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1105G>A
  hgvsp: ENSP00000432877.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1105G>A
  hgvsp: ENSP00000432851.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1096G>A
  hgvsp: ENSP00000410825.2:p.Ala366Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*174G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1105G>A
  hgvsp: ENSP00000434816.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1105G>A
  hgvsp: ENSP00000435055.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1105G>A
  hgvsp: ENSP00000339992.5:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1105G>A
  hgvsp: ENSP00000432168.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1105G>A
  hgvsp: ENSP00000356788.4:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1096G>A
  hgvsp: ENSP00000433458.1:p.Ala366Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*174G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1096G>A
  hgvsp: ENSP00000433844.1:p.Ala366Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*694G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1105G>A
  hgvsp: ENSP00000435293.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1221G>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala369Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

6-135517053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517053
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517053
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1116A>G
  hgvsp: ENST00000438901.2:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*185A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.168A>G
  hgvsp: ENST00000534736.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*185A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1116A>G
  hgvsp: ENST00000367812.2:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1116A>G
  hgvsp: ENST00000528015.1:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1455A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1116A>G
  hgvsp: ENST00000528140.1:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1116A>G
  hgvsp: ENST00000525940.1:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1116A>G
  hgvsp: ENST00000367814.4:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1107A>G
  hgvsp: ENST00000528774.1:c.1107A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1107A>G
  hgvsp: ENST00000442647.2:c.1107A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1116A>G
  hgvsp: ENST00000531737.1:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1116A>G
  hgvsp: ENST00000316528.8:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1116A>G
  hgvsp: ENST00000526320.1:c.1116A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1107A>G
  hgvsp: ENST00000529262.1:c.1107A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1107A>G
  hgvsp: ENST00000526187.1:c.1107A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.*185A>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

6-135517059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517059
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517059
    reference: chr 6
allele count: 387
allele frequency: 3.189017255302668e-3
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1122C>T
  hgvsp: ENST00000527615.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1118+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1118+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1118+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1122C>T
  hgvsp: ENST00000525002.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.75G>A
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1122C>T
  hgvsp: ENST00000534044.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1118+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1461C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*191C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1122C>T
  hgvsp: ENST00000534121.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1122C>T
  hgvsp: ENST00000341911.5:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*589C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+4C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1017C>T
  hgvsp: ENST00000533624.1:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*191C>T
  variant of: http://identifiers.org/hgnc/7545
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.*187+4C>T
num of homozygotes: 6
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

6-135517063-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517063
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517063
    reference: chr 6
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1117A>T
  hgvsp: ENSP00000410825.2:p.Ile373Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1242A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1126A>T
  hgvsp: ENSP00000339992.5:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1126A>T
  hgvsp: ENSP00000434639.1:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1126A>T
  hgvsp: ENSP00000356786.2:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1117A>T
  hgvsp: ENSP00000434723.1:p.Ile373Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*715A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*187+8A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1126A>T
  hgvsp: ENSP00000435055.1:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1021A>T
  hgvsp: ENSP00000436605.1:p.Ile341Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1126A>T
  hgvsp: ENSP00000356788.4:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1126A>T
  hgvsp: ENSP00000433227.1:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1126A>T
  hgvsp: ENSP00000433745.1:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1126A>T
  hgvsp: ENSP00000432851.1:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1126A>T
  hgvsp: ENSP00000341050.5:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1126A>T
  hgvsp: ENSP00000413011.2:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+8A>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1126A>T
  hgvsp: ENSP00000435293.1:p.Ile376Phe
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile376Phe
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

6-135517065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517065
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517065
    reference: chr 6
allele count: 5
allele frequency: 4.119905736556747e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1128C>T
  hgvsp: ENST00000316528.8:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1128C>T
  hgvsp: ENST00000438901.2:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1119C>T
  hgvsp: ENST00000526889.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1128C>T
  hgvsp: ENST00000341911.5:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*197C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1023C>T
  hgvsp: ENST00000533624.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*197C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.180C>T
  hgvsp: ENST00000534736.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1128C>T
  hgvsp: ENST00000527615.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*187+10C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*197C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1128C>T
  hgvsp: ENST00000525002.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1128C>T
  hgvsp: ENST00000533808.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+10C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*717C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1119C>T
  hgvsp: ENST00000442647.2:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1128C>T
  hgvsp: ENST00000367812.2:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1128C>T
  hgvsp: ENST00000339290.5:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile376Ile
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

6-135517070-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517070
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517070
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1133A>G
  hgvsp: ENSP00000356786.2:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1124A>G
  hgvsp: ENSP00000410825.2:p.His375Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*202A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1133A>G
  hgvsp: ENSP00000339992.5:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1133A>G
  hgvsp: ENSP00000356788.4:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1133A>G
  hgvsp: ENSP00000341050.5:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*187+15A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1133A>G
  hgvsp: ENSP00000434420.1:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*600A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1133A>G
  hgvsp: ENSP00000433227.1:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+15A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1133A>G
  hgvsp: ENSP00000432851.1:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1133A>G
  hgvsp: ENSP00000433745.1:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.185A>G
  hgvsp: ENSP00000432042.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+15A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*202A>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1133A>G
  hgvsp: ENSP00000435293.1:p.His378Arg
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1028A>G
  hgvsp: ENSP00000436605.1:p.His343Arg
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His378Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-135517076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517076
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517076
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1139G>A
  hgvsp: ENSP00000435055.1:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*208G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1118+21G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1139G>A
  hgvsp: ENSP00000413011.2:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1118+21G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1139G>A
  hgvsp: ENSP00000326328.8:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.191G>A
  hgvsp: ENSP00000432042.1:p.Gly64Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1130G>A
  hgvsp: ENSP00000410825.2:p.Gly377Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1139G>A
  hgvsp: ENSP00000341050.5:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1139G>A
  hgvsp: ENSP00000435293.1:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*208G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1034G>A
  hgvsp: ENSP00000436605.1:p.Gly345Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1139G>A
  hgvsp: ENSP00000356786.2:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.58C>T
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1139G>A
  hgvsp: ENSP00000432811.1:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*728G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1139G>A
  hgvsp: ENSP00000432851.1:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1255G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1139G>A
  hgvsp: ENSP00000434420.1:p.Gly380Asp
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly380Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

6-135517092-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517092
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517092
    reference: chr 6
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1155T>C
  hgvsp: ENST00000367814.4:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.207T>C
  hgvsp: ENST00000534736.1:c.207T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000236703
  ensembl transcript: ENST00000455534
  gene symbol: MYB-AS1
  hgvsc: ENST00000455534.1:n.42A>G
  variant of: http://identifiers.org/hgnc/37457
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436925
  ensembl transcript: ENST00000531634
  gene symbol: MYB
  hgvsc: ENST00000531634.1:c.*744T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*224T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*224T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1155T>C
  hgvsp: ENST00000341911.5:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1155T>C
  hgvsp: ENST00000525002.1:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+37T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1494T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1155T>C
  hgvsp: ENST00000438901.2:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1146T>C
  hgvsp: ENST00000526889.1:c.1146T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1155T>C
  hgvsp: ENST00000527615.1:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1155T>C
  hgvsp: ENST00000533808.1:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1146T>C
  hgvsp: ENST00000528774.1:c.1146T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1146T>C
  hgvsp: ENST00000442647.2:c.1146T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*224T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1155T>C
  hgvsp: ENST00000533837.1:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1155T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-135517097-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517097
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517097
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1151A>C
  hgvsp: ENSP00000433458.1:p.Lys384Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+42A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1160A>C
  hgvsp: ENSP00000339992.5:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1160A>C
  hgvsp: ENSP00000435055.1:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1160A>C
  hgvsp: ENSP00000326328.8:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1160A>C
  hgvsp: ENSP00000434420.1:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*229A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1160A>C
  hgvsp: ENSP00000341050.5:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1160A>C
  hgvsp: ENSP00000433227.1:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+42A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1276A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1055A>C
  hgvsp: ENSP00000436605.1:p.Lys352Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1151A>C
  hgvsp: ENSP00000410825.2:p.Lys384Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1151A>C
  hgvsp: ENSP00000434723.1:p.Lys384Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1499A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*229A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1118+42A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1160A>C
  hgvsp: ENSP00000433745.1:p.Lys387Thr
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*229A>C
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys387Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

6-135517130-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517130
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517130
    reference: chr 6
allele count: 2
allele frequency: 1.651609493451368e-5
allele num: 121094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1193T>G
  hgvsp: ENSP00000356788.4:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1184T>G
  hgvsp: ENSP00000434723.1:p.Phe395Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1193T>G
  hgvsp: ENSP00000356786.2:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1193T>G
  hgvsp: ENSP00000433745.1:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*262T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.245T>G
  hgvsp: ENSP00000432042.1:p.Phe82Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1088T>G
  hgvsp: ENSP00000436605.1:p.Phe363Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*262T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1118+75T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1184T>G
  hgvsp: ENSP00000433458.1:p.Phe395Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1193T>G
  hgvsp: ENSP00000435293.1:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1193T>G
  hgvsp: ENSP00000341050.5:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1155+38T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*262T>G
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1193T>G
  hgvsp: ENSP00000434420.1:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1193T>G
  hgvsp: ENSP00000433227.1:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1193T>G
  hgvsp: ENSP00000432811.1:p.Phe398Cys
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1118+75T>G
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe398Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

6-135517137-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517137
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517137
    reference: chr 6
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1200T>C
  hgvsp: ENST00000341911.5:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1095T>C
  hgvsp: ENST00000533624.1:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1316T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1200T>C
  hgvsp: ENST00000339290.5:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*269T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1191T>C
  hgvsp: ENST00000528774.1:c.1191T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1200T>C
  hgvsp: ENST00000527615.1:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*269T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1200T>C
  hgvsp: ENST00000367812.2:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1200T>C
  hgvsp: ENST00000525002.1:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1200T>C
  hgvsp: ENST00000528343.1:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1539T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432811
  ensembl transcript: ENST00000533384
  gene symbol: MYB
  hgvsc: ENST00000533384.1:c.1200T>C
  hgvsp: ENST00000533384.1:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1200T>C
  hgvsp: ENST00000316528.8:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1118+82T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1539T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.252T>C
  hgvsp: ENST00000534736.1:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1118+82T>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1200T>C
  hgvsp: ENST00000534044.1:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp400Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-135517147-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517147
    reference: chr 6
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1203+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+92A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1203+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1203+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433458
  ensembl transcript: ENST00000526889
  gene symbol: MYB
  hgvsc: ENST00000526889.1:c.1194+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435938
  ensembl transcript: ENST00000525369
  gene symbol: MYB
  hgvsc: ENST00000525369.1:c.948+1549A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+92A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.255+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1118+92A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*187+92A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1194+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*272+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*272+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1319+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*272+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1203+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1203+7A>C
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*272+7A>C
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1203+7A>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

6-135517160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517160
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517160
    reference: chr 6
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1194+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*272+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+105G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1562G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*272+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1098+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*272+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1118+105G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+105G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1194+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432948
  ensembl transcript: ENST00000525940
  gene symbol: MYB
  hgvsc: ENST00000525940.1:c.1118+105G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*272+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1319+20G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1203+20G>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-135517163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517163
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517163
    reference: chr 6
allele count: 5
allele frequency: 4.160495265356388e-5
allele num: 120178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1155+71G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*670+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437081
  ensembl transcript: ENST00000525477
  gene symbol: MYB
  hgvsc: ENST00000525477.1:c.*272+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1203+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*272+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1203+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1194+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1118+108G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*272+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1203+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1203+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432042
  ensembl transcript: ENST00000534736
  gene symbol: MYB
  hgvsc: ENST00000534736.1:c.255+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+108G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1098+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1319+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1203+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1203+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+108G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435497
  ensembl transcript: ENST00000528345
  gene symbol: MYB
  hgvsc: ENST00000528345.1:c.*272+23G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1118+108G>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-135517168-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517168
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517168
    reference: chr 6
allele count: 1
allele frequency: 8.338614455822021e-6
allele num: 119924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*187+113C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1118+113C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1319+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1194+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1570C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+113C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+113C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1203+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*272+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*272+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1098+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436602
  ensembl transcript: ENST00000463282
  gene symbol: MYB
  hgvsc: ENST00000463282.2:c.*272+28C>T
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432168
  ensembl transcript: ENST00000531737
  gene symbol: MYB
  hgvsc: ENST00000531737.1:c.1118+113C>T
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-135517168-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517168
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517167
    reference: chr 6
allele count: 1
allele frequency: 8.338614455822021e-6
allele num: 119924
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+114delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434795
  ensembl transcript: ENST00000526187
  gene symbol: MYB
  hgvsc: ENST00000526187.1:c.1109+114delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436605
  ensembl transcript: ENST00000533624
  gene symbol: MYB
  hgvsc: ENST00000533624.1:c.1098+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1319+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1155+77delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434816
  ensembl transcript: ENST00000528015
  gene symbol: MYB
  hgvsc: ENST00000528015.1:c.1118+114delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356788
  ensembl transcript: ENST00000367814
  gene symbol: MYB
  hgvsc: ENST00000367814.4:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1118+114delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000437264
  ensembl transcript: ENST00000529586
  gene symbol: MYB
  hgvsc: ENST00000529586.1:c.*187+114delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433745
  ensembl transcript: ENST00000525002
  gene symbol: MYB
  hgvsc: ENST00000525002.1:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1203+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1194+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434675
  ensembl transcript: ENST00000524588
  gene symbol: MYB
  hgvsc: ENST00000524588.1:c.*670+29delG
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1194+29delG
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: CG
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-135517169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135517169
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 135517169
    reference: chr 6
allele count: 1
allele frequency: 8.346827370916315e-6
allele num: 119806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434917
  ensembl transcript: ENST00000526320
  gene symbol: MYB
  hgvsc: ENST00000526320.1:c.1118+114G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434639
  ensembl transcript: ENST00000533837
  gene symbol: MYB
  hgvsc: ENST00000533837.1:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl transcript: ENST00000531845
  gene symbol: MYB
  hgvsc: ENST00000531845.1:n.1319+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433227
  ensembl transcript: ENST00000527615
  gene symbol: MYB
  hgvsc: ENST00000527615.1:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000339992
  ensembl transcript: ENST00000341911
  gene symbol: MYB
  hgvsc: ENST00000341911.5:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000433844
  ensembl transcript: ENST00000529262
  gene symbol: MYB
  hgvsc: ENST00000529262.1:c.1109+114G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000356786
  ensembl transcript: ENST00000367812
  gene symbol: MYB
  hgvsc: ENST00000367812.2:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435293
  ensembl transcript: ENST00000533808
  gene symbol: MYB
  hgvsc: ENST00000533808.1:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435595
  ensembl transcript: ENST00000531519
  gene symbol: MYB
  hgvsc: ENST00000531519.1:c.948+1571G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434420
  ensembl transcript: ENST00000528343
  gene symbol: MYB
  hgvsc: ENST00000528343.1:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000410825
  ensembl transcript: ENST00000442647
  gene symbol: MYB
  hgvsc: ENST00000442647.2:c.1194+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000341050
  ensembl transcript: ENST00000339290
  gene symbol: MYB
  hgvsc: ENST00000339290.5:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435578
  ensembl transcript: ENST00000525514
  gene symbol: MYB
  hgvsc: ENST00000525514.1:c.*272+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000436385
  ensembl transcript: ENST00000526565
  gene symbol: MYB
  hgvsc: ENST00000526565.1:c.*272+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000413011
  ensembl transcript: ENST00000438901
  gene symbol: MYB
  hgvsc: ENST00000438901.2:c.1155+77G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432851
  ensembl transcript: ENST00000534121
  gene symbol: MYB
  hgvsc: ENST00000534121.1:c.1155+77G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000432877
  ensembl transcript: ENST00000528140
  gene symbol: MYB
  hgvsc: ENST00000528140.1:c.1118+114G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000434723
  ensembl transcript: ENST00000528774
  gene symbol: MYB
  hgvsc: ENST00000528774.1:c.1194+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000435055
  ensembl transcript: ENST00000534044
  gene symbol: MYB
  hgvsc: ENST00000534044.1:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118513
  ensembl protein: ENSP00000326328
  ensembl transcript: ENST00000316528
  gene symbol: MYB
  hgvsc: ENST00000316528.8:c.1203+29G>A
  variant of: http://identifiers.org/hgnc/7545
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
num of homozygotes: 0
reference allele: G

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*18-6_*18-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*18-6_*18-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*18-6_*18-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.844-6_844-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*18-6_*18-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*18-6_*18-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*18-6_*18-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.940-6_940-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1282_948+1285delCCTT
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.949-6_949-3delCCTT
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 306
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6575
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16539
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1198
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5842
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8658
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3673
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13235
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 582
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7273
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14371
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3399
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

QD
type: SiteQuality
SIO_000300: 1.701e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

DP
type: SiteQuality
SIO_000300: 2.144668e6

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*18-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*18-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.949-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*18-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.949-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.949-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.949-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1065-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*18-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.940-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.949-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.940-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+155G>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.949-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*538-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*18-10C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*416-10C>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 307
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16545
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13246
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 582
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6571
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5837
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 156
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3668
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8654
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20929
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7273
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14365
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.046993780234969e-4
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.31e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.061e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.712e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

DP
type: SiteQuality
SIO_000300: 2.144953e6

FS
type: SiteQuality
SIO_000300: 3.752e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.11e-1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1281T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1281T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*416-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1065-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+152A>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.940-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*18-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.940-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*18-7T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.949-7T>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3667
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1197
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6577
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 581
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8652
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16564
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5835
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13248
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7278
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20970
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4985
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.82e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.46e-1

FS
type: SiteQuality
SIO_000300: 1.552e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.144787e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.940A>T
hgvsp: ENSP00000410825.2:p.Thr314Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.940A>T
hgvsp: ENSP00000434795.1:p.Thr314Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1288A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.949A>T
hgvsp: ENSP00000433745.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.949A>T
hgvsp: ENSP00000326328.8:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.949A>T
hgvsp: ENSP00000432851.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.949A>T
hgvsp: ENSP00000432877.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.940A>T
hgvsp: ENSP00000433458.1:p.Thr314Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.949A>T
hgvsp: ENSP00000434639.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*538A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1065A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*18A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.949A>T
hgvsp: ENSP00000434816.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.949A>T
hgvsp: ENSP00000339992.5:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.949A>T
hgvsp: ENSP00000341050.5:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.949A>T
hgvsp: ENSP00000435055.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.949A>T
hgvsp: ENSP00000435293.1:p.Thr317Ser
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*416A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*18A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*18A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*18A>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8646
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2076
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6568
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5837
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3669
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16594
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13244
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14358
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 20989
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997422216893472e-5
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.145036e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.965G>A
hgvsp: ENSP00000433745.1:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.965G>A
hgvsp: ENSP00000432168.1:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+129C>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.965G>A
hgvsp: ENSP00000434639.1:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.965G>A
hgvsp: ENSP00000432811.1:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.965G>A
hgvsp: ENSP00000434816.1:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.965G>A
hgvsp: ENSP00000356786.2:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.965G>A
hgvsp: ENSP00000341050.5:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.965G>A
hgvsp: ENSP00000413011.2:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*34G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1081G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.965G>A
hgvsp: ENSP00000356788.4:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*34G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*34G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*554G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*34G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1304G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.965G>A
hgvsp: ENSP00000432877.1:p.Cys322Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.956G>A
hgvsp: ENSP00000434723.1:p.Cys319Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.956G>A
hgvsp: ENSP00000410825.2:p.Cys319Tyr
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 13248
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6550
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 272
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 16635
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3667
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5826
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8642
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14359
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991188635137565e-5
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.407e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.105e1

DP
type: SiteQuality
SIO_000300: 2.145564e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.970T>G
hgvsp: ENSP00000435055.1:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.970T>G
hgvsp: ENSP00000434917.1:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*39T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.970T>G
hgvsp: ENSP00000356786.2:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*437T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*39T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.961T>G
hgvsp: ENSP00000434795.1:p.Tyr321Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.970T>G
hgvsp: ENSP00000432948.1:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.961T>G
hgvsp: ENSP00000434723.1:p.Tyr321Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+124A>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.22T>G
hgvsp: ENSP00000432042.1:p.Tyr8Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1086T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.970T>G
hgvsp: ENSP00000356788.4:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.970T>G
hgvsp: ENSP00000432877.1:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*39T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1309T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*39T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.970T>G
hgvsp: ENSP00000433745.1:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.970T>G
hgvsp: ENSP00000433227.1:p.Tyr324Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.865T>G
hgvsp: ENSP00000436605.1:p.Tyr289Asp
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 581
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8643
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1194
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5827
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16646
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6550
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13251
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14351
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21052
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7290
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.085e1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 1.187e0

DP
type: SiteQuality
SIO_000300: 2.144918e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.974C>A
hgvsp: ENSP00000326328.8:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.974C>A
hgvsp: ENSP00000434639.1:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*43C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*43C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*441C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.965C>A
hgvsp: ENSP00000434723.1:p.Pro322His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*563C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*43C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.26C>A
hgvsp: ENSP00000432042.1:p.Pro9His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1313C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.965C>A
hgvsp: ENSP00000433458.1:p.Pro322His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*43C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.974C>A
hgvsp: ENSP00000356788.4:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.974C>A
hgvsp: ENSP00000434420.1:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.965C>A
hgvsp: ENSP00000433844.1:p.Pro322His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.974C>A
hgvsp: ENSP00000433227.1:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*43C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.974C>A
hgvsp: ENSP00000432877.1:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.974C>A
hgvsp: ENSP00000413011.2:p.Pro325His
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1313C>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 13253
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16650
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8645
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5825
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1194
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3666
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21058
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.603e0

DP
type: SiteQuality
SIO_000300: 2.144964e6

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.424e0

QD
type: SiteQuality
SIO_000300: 1.413e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.975C>G
hgvsp: ENST00000341911.5:c.975C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.966C>G
hgvsp: ENST00000526187.1:c.966C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.27C>G
hgvsp: ENST00000534736.1:c.27C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*44C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.975C>G
hgvsp: ENST00000525940.1:c.975C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*44C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.966C>G
hgvsp: ENST00000529262.1:c.966C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*44C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1314C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.975C>G
hgvsp: ENST00000316528.8:c.975C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*44C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.975C>G
hgvsp: ENST00000528343.1:c.975C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.975C>G
hgvsp: ENST00000367812.2:c.975C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1091C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*564C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1314C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*44C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*442C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.975C>G
hgvsp: ENST00000526320.1:c.975C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*44C>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 16654
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13252
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2074
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5825
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8644
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14349
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.348e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 4.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

DP
type: SiteQuality
SIO_000300: 2.145189e6

QD
type: SiteQuality
SIO_000300: 1.178e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.966C>T
hgvsp: ENST00000529262.1:c.966C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.966C>T
hgvsp: ENST00000442647.2:c.966C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.975C>T
hgvsp: ENST00000339290.5:c.975C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*44C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1091C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*442C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*44C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.975C>T
hgvsp: ENST00000533384.1:c.975C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.975C>T
hgvsp: ENST00000527615.1:c.975C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*564C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1314C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*44C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.27C>T
hgvsp: ENST00000534736.1:c.27C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*44C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.966C>T
hgvsp: ENST00000528774.1:c.966C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+119G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.966C>T
hgvsp: ENST00000526889.1:c.966C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1314C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.975C>T
hgvsp: ENST00000528343.1:c.975C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*44C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13252
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5825
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16654
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8644
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 256
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2074
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14349
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 4.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.348e0

DP
type: SiteQuality
SIO_000300: 2.145189e6

QD
type: SiteQuality
SIO_000300: 1.178e1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*45G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.976G>A
hgvsp: ENSP00000434816.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.976G>A
hgvsp: ENSP00000435293.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.967G>A
hgvsp: ENSP00000433844.1:p.Gly323Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.976G>A
hgvsp: ENSP00000435055.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.976G>A
hgvsp: ENSP00000432851.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.976G>A
hgvsp: ENSP00000356788.4:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1092G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.976G>A
hgvsp: ENSP00000434639.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*45G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.976G>A
hgvsp: ENSP00000434420.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*443G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.976G>A
hgvsp: ENSP00000432168.1:p.Gly326Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1315G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1315G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+118C>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*45G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.28G>A
hgvsp: ENSP00000432042.1:p.Gly10Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.967G>A
hgvsp: ENSP00000434723.1:p.Gly323Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.967G>A
hgvsp: ENSP00000410825.2:p.Gly323Arg
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 267
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5829
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6545
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8643
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2076
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16655
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7291
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.144898e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.209e0

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.814e0

FS
type: SiteQuality
SIO_000300: 3.048e0

VQSLOD
type: SiteQuality
SIO_000300: -3.197e0

QD
type: SiteQuality
SIO_000300: 2.291e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.986G>A
hgvsp: ENSP00000435055.1:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*55G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.38G>A
hgvsp: ENSP00000432042.1:p.Ser13Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.986G>A
hgvsp: ENSP00000341050.5:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*55G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.986G>A
hgvsp: ENSP00000433227.1:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.986G>A
hgvsp: ENSP00000356786.2:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+108C>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*453G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.977G>A
hgvsp: ENSP00000434723.1:p.Ser326Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.986G>A
hgvsp: ENSP00000413011.2:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.986G>A
hgvsp: ENSP00000432811.1:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.986G>A
hgvsp: ENSP00000435293.1:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.986G>A
hgvsp: ENSP00000434420.1:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1325G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1325G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*55G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*55G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.986G>A
hgvsp: ENSP00000433745.1:p.Ser329Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.977G>A
hgvsp: ENSP00000410825.2:p.Ser326Asn
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 5826
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16657
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 752
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8647
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2076
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6542
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13254
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7290
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14344
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.358e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 2.144953e6

QD
type: SiteQuality
SIO_000300: 7.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.819e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.984C>T
hgvsp: ENST00000442647.2:c.984C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*62C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*62C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.993C>T
hgvsp: ENST00000525002.1:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*62C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.984C>T
hgvsp: ENST00000528774.1:c.984C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.993C>T
hgvsp: ENST00000339290.5:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*582C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.993C>T
hgvsp: ENST00000367812.2:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.993C>T
hgvsp: ENST00000316528.8:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+101G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.993C>T
hgvsp: ENST00000438901.2:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1332C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*62C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*62C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*62C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*460C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.993C>T
hgvsp: ENST00000531737.1:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1109C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.993C>T
hgvsp: ENST00000367814.4:c.993C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16656
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5826
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8649
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13253
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2076
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3663
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 256
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

QD
type: SiteQuality
SIO_000300: 1.521e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.792e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 2.144949e6

FS
type: SiteQuality
SIO_000300: 4.383e0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.999C>T
hgvsp: ENST00000438901.2:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.999C>T
hgvsp: ENST00000341911.5:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*68C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*68C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.990C>T
hgvsp: ENST00000526187.1:c.990C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.51C>T
hgvsp: ENST00000534736.1:c.51C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*466C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.999C>T
hgvsp: ENST00000525940.1:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.990C>T
hgvsp: ENST00000442647.2:c.990C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.999C>T
hgvsp: ENST00000528343.1:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.990C>T
hgvsp: ENST00000526889.1:c.990C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.999C>T
hgvsp: ENST00000527615.1:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.999C>T
hgvsp: ENST00000316528.8:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*588C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1338C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+95G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*68C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*68C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.999C>T
hgvsp: ENST00000367812.2:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1115C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6544
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16654
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8649
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13255
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5823
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7280
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14339
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.402e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 2.144776e6

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 9.27e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1000G>A
hgvsp: ENSP00000356786.2:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*589G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1000G>A
hgvsp: ENSP00000339992.5:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1000G>A
hgvsp: ENSP00000432851.1:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1000G>A
hgvsp: ENSP00000341050.5:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.991G>A
hgvsp: ENSP00000433458.1:p.Asp331Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*69G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1000G>A
hgvsp: ENSP00000433227.1:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1116G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*69G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1000G>A
hgvsp: ENSP00000433745.1:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.52G>A
hgvsp: ENSP00000432042.1:p.Asp18Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*69G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1000G>A
hgvsp: ENSP00000432811.1:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1000G>A
hgvsp: ENSP00000432168.1:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1000G>A
hgvsp: ENSP00000413011.2:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*69G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1000G>A
hgvsp: ENSP00000434816.1:p.Asp334Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1339G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+94C>T
variant of: http://identifiers.org/hgnc/37457

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3666
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16653
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8653
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13256
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5822
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6539
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 255
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7279
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14339
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.211e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.144909e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1003C>T
hgvsp: ENSP00000432168.1:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*72C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1003C>T
hgvsp: ENSP00000433227.1:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*72C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1003C>T
hgvsp: ENSP00000432948.1:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.55C>T
hgvsp: ENSP00000432042.1:p.His19Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1003C>T
hgvsp: ENSP00000413011.2:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.994C>T
hgvsp: ENSP00000433844.1:p.His332Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1003C>T
hgvsp: ENSP00000432851.1:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.994C>T
hgvsp: ENSP00000410825.2:p.His332Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.994C>T
hgvsp: ENSP00000433458.1:p.His332Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.898C>T
hgvsp: ENSP00000436605.1:p.His300Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*592C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1342C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*72C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*72C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.994C>T
hgvsp: ENSP00000434795.1:p.His332Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1342C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1003C>T
hgvsp: ENSP00000434816.1:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1003C>T
hgvsp: ENSP00000356788.4:p.His335Tyr
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 754
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1194
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8652
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2073
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6542
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5824
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16655
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13256
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3664
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.59e0

QD
type: SiteQuality
SIO_000300: 1.211e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.14473e6

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.996C>G
hgvsp: ENSP00000434795.1:p.His332Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1005C>G
hgvsp: ENSP00000356786.2:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*74C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.996C>G
hgvsp: ENSP00000433844.1:p.His332Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1005C>G
hgvsp: ENSP00000356788.4:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.900C>G
hgvsp: ENSP00000436605.1:p.His300Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1005C>G
hgvsp: ENSP00000433745.1:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1005C>G
hgvsp: ENSP00000432811.1:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*472C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*594C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.57C>G
hgvsp: ENSP00000432042.1:p.His19Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*74C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.996C>G
hgvsp: ENSP00000434723.1:p.His332Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1344C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1344C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*74C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1005C>G
hgvsp: ENSP00000434420.1:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+89G>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1005C>G
hgvsp: ENSP00000432168.1:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1005C>G
hgvsp: ENSP00000433227.1:p.His335Gln
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 5823
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 409
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8650
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6537
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13256
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16657
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3663
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2074
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14338
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 1.188e0

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

DP
type: SiteQuality
SIO_000300: 2.144661e6

QD
type: SiteQuality
SIO_000300: 1.492e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1007C>T
hgvsp: ENSP00000356786.2:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.998C>T
hgvsp: ENSP00000433844.1:p.Thr333Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1007C>T
hgvsp: ENSP00000434917.1:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*76C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*76C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.998C>T
hgvsp: ENSP00000433458.1:p.Thr333Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.59C>T
hgvsp: ENSP00000432042.1:p.Thr20Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1007C>T
hgvsp: ENSP00000413011.2:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*76C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1007C>T
hgvsp: ENSP00000432877.1:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1007C>T
hgvsp: ENSP00000435293.1:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1346C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1007C>T
hgvsp: ENSP00000341050.5:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*76C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*76C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1007C>T
hgvsp: ENSP00000433745.1:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1007C>T
hgvsp: ENSP00000434420.1:p.Thr336Ile
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+87G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.998C>T
hgvsp: ENSP00000434723.1:p.Thr333Ile
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 13245
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 159
bin: 8.75e1
variant carriers: 7

GenotypeDepth
all individuals: 575
bin: 6.75e1
variant carriers: 5

GenotypeDepth
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 310
bin: 7.75e1
variant carriers: 8

GenotypeDepth
all individuals: 16656
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8650
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 6530
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 6.25e1
variant carriers: 9

GenotypeDepth
all individuals: 3648
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1185
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 118
bin: 9.25e1
variant carriers: 9

GenotypeDepth
all individuals: 317
bin: 9.75e1
variant carriers: 56

GenotypeDepth
all individuals: 5810
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2066
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 413
bin: 7.25e1
variant carriers: 7

GenotypeDepth
all individuals: 255
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3398
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14360
bin: 9.75e1
variant carriers: 124

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 120
allele frequency: 1.153180857197771e-2
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.262e1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

DP
type: SiteQuality
SIO_000300: 2.150934e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.569e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1008C>G
hgvsp: ENST00000525940.1:c.1008C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1347C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.999C>G
hgvsp: ENST00000442647.2:c.999C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1008C>G
hgvsp: ENST00000341911.5:c.1008C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1124C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.903C>G
hgvsp: ENST00000533624.1:c.903C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1008C>G
hgvsp: ENST00000339290.5:c.1008C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+86G>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*77C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*77C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*77C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.999C>G
hgvsp: ENST00000526889.1:c.999C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1008C>G
hgvsp: ENST00000367814.4:c.1008C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*597C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*77C>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.999C>G
hgvsp: ENST00000529262.1:c.999C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.999C>G
hgvsp: ENST00000526187.1:c.999C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1008C>G
hgvsp: ENST00000525002.1:c.1008C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1008C>G
hgvsp: ENST00000316528.8:c.1008C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*475C>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 13256
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6536
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3663
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5820
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8664
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16693
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2069
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21097
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7289
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.964e0

QD
type: SiteQuality
SIO_000300: 1.28e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.711e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

DP
type: SiteQuality
SIO_000300: 2.142687e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1008C>T
hgvsp: ENST00000534044.1:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1008C>T
hgvsp: ENST00000341911.5:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.999C>T
hgvsp: ENST00000526889.1:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1008C>T
hgvsp: ENST00000525002.1:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*77C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.60C>T
hgvsp: ENST00000534736.1:c.60C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.903C>T
hgvsp: ENST00000533624.1:c.903C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1008C>T
hgvsp: ENST00000367812.2:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.999C>T
hgvsp: ENST00000528774.1:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1008C>T
hgvsp: ENST00000339290.5:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*475C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1347C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*77C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+86G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*77C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1008C>T
hgvsp: ENST00000531737.1:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1008C>T
hgvsp: ENST00000438901.2:c.1008C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1124C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*77C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*597C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3663
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16693
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1185
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6536
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8664
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2069
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13256
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5820
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7289
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21097
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.711e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.964e0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 2.142687e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1009A>G
hgvsp: ENSP00000434917.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1009A>G
hgvsp: ENSP00000432948.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*78A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1009A>G
hgvsp: ENSP00000435293.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*598A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1009A>G
hgvsp: ENSP00000326328.8:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.904A>G
hgvsp: ENSP00000436605.1:p.Arg302Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1009A>G
hgvsp: ENSP00000433745.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1009A>G
hgvsp: ENSP00000433227.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*78A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*78A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1000A>G
hgvsp: ENSP00000434723.1:p.Arg334Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1009A>G
hgvsp: ENSP00000432168.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1000A>G
hgvsp: ENSP00000433844.1:p.Arg334Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1009A>G
hgvsp: ENSP00000413011.2:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1000A>G
hgvsp: ENSP00000433458.1:p.Arg334Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.61A>G
hgvsp: ENSP00000432042.1:p.Arg21Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1009A>G
hgvsp: ENSP00000432811.1:p.Arg337Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*78A>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 13257
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1185
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8665
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16695
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6536
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5818
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2067
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14279
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21097
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4989
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

QD
type: SiteQuality
SIO_000300: 1.675e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 2.142517e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.368e0

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1017T>G
hgvsp: ENSP00000435293.1:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1008T>G
hgvsp: ENSP00000410825.2:p.His336Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*86T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*484T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*86T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+77A>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*86T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1017T>G
hgvsp: ENSP00000341050.5:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1017T>G
hgvsp: ENSP00000434420.1:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*86T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1133T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*606T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1017T>G
hgvsp: ENSP00000433227.1:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1017T>G
hgvsp: ENSP00000432877.1:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*86T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1017T>G
hgvsp: ENSP00000432168.1:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1008T>G
hgvsp: ENSP00000433844.1:p.His336Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1017T>G
hgvsp: ENSP00000432851.1:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1356T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1017T>G
hgvsp: ENSP00000356786.2:p.His339Gln
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8660
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16689
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2068
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6530
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1187
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5818
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13259
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 572
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.95e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

QD
type: SiteQuality
SIO_000300: 1.499e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.978e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

DP
type: SiteQuality
SIO_000300: 2.142392e6

VQSLOD
type: SiteQuality
SIO_000300: -1.212e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

Annotation
canonical: true
clinical significance: not_provided
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1037C>T
hgvsp: ENSP00000339992.5:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1037C>T
hgvsp: ENSP00000432168.1:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1037C>T
hgvsp: ENSP00000432851.1:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1037C>T
hgvsp: ENSP00000432948.1:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1037C>T
hgvsp: ENSP00000434816.1:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*504C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1028C>T
hgvsp: ENSP00000433844.1:p.Ser343Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1376C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*106C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1028C>T
hgvsp: ENSP00000410825.2:p.Ser343Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1037C>T
hgvsp: ENSP00000413011.2:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1037C>T
hgvsp: ENSP00000435055.1:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1153C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*106C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1376C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.89C>T
hgvsp: ENSP00000432042.1:p.Ser30Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
clinical significance: not_provided
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+57G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
clinical significance: not_provided
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*626C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1028C>T
hgvsp: ENSP00000434723.1:p.Ser343Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1037C>T
hgvsp: ENSP00000433745.1:p.Ser346Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
clinical significance: not_provided
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*106C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13254
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1185
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6518
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16705
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2066
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 572
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8658
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3660
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5810
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14278
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7280
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.367e0

VQSLOD
type: SiteQuality
SIO_000300: -3.326e0

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

FS
type: SiteQuality
SIO_000300: 1.6379e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.641e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.987e1

DP
type: SiteQuality
SIO_000300: 2.142087e6

QD
type: SiteQuality
SIO_000300: 1.265e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1046G>A
hgvsp: ENSP00000432851.1:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1046G>A
hgvsp: ENSP00000434639.1:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1046G>A
hgvsp: ENSP00000341050.5:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1037G>A
hgvsp: ENSP00000434795.1:p.Gly346Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1037G>A
hgvsp: ENSP00000433844.1:p.Gly346Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1046G>A
hgvsp: ENSP00000434816.1:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1037G>A
hgvsp: ENSP00000410825.2:p.Gly346Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1046G>A
hgvsp: ENSP00000432948.1:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*115G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1046G>A
hgvsp: ENSP00000356786.2:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.98G>A
hgvsp: ENSP00000432042.1:p.Gly33Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*513G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1162G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*115G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1037G>A
hgvsp: ENSP00000434723.1:p.Gly346Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1385G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1046G>A
hgvsp: ENSP00000432811.1:p.Gly349Glu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*635G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*115G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1385G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8659
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6526
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 572
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3653
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5796
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2066
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13251
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16705
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1185
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.105e-1

FS
type: SiteQuality
SIO_000300: 8.433e0

DP
type: SiteQuality
SIO_000300: 2.141227e6

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1049A>G
hgvsp: ENSP00000413011.2:p.Glu350Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*118A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1049A>G
hgvsp: ENSP00000434420.1:p.Glu350Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1049A>G
hgvsp: ENSP00000356786.2:p.Glu350Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1040A>G
hgvsp: ENSP00000433844.1:p.Glu347Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*118A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1049A>G
hgvsp: ENSP00000435055.1:p.Glu350Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+45T>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1049A>G
hgvsp: ENSP00000433745.1:p.Glu350Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1388A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1388A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1040A>G
hgvsp: ENSP00000434795.1:p.Glu347Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*638A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1049A>G
hgvsp: ENSP00000341050.5:p.Glu350Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1040A>G
hgvsp: ENSP00000433458.1:p.Glu347Gly
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*118A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*118A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*118A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1165A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1040A>G
hgvsp: ENSP00000434723.1:p.Glu347Gly
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 3650
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6530
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 572
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2067
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8655
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13245
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16714
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5793
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1183
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7276
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14259
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.140933e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-1

QD
type: SiteQuality
SIO_000300: 1.248e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

FS
type: SiteQuality
SIO_000300: 1.865e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1051C>A
hgvsp: ENSP00000432851.1:p.His351Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1042C>A
hgvsp: ENSP00000433458.1:p.His348Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*120C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1051C>A
hgvsp: ENSP00000432877.1:p.His351Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1390C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+43G>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1042C>A
hgvsp: ENSP00000410825.2:p.His348Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*120C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1042C>A
hgvsp: ENSP00000434723.1:p.His348Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1390C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*518C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*120C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*640C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1051C>A
hgvsp: ENSP00000433227.1:p.His351Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*120C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1051C>A
hgvsp: ENSP00000413011.2:p.His351Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*120C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1167C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1051C>A
hgvsp: ENSP00000356788.4:p.His351Asn
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1051C>A
hgvsp: ENSP00000433745.1:p.His351Asn
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 3654
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6530
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5793
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 572
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2065
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16716
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8655
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13238
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7273
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3393
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14259
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.82e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.519e0

QD
type: SiteQuality
SIO_000300: 1.431e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

DP
type: SiteQuality
SIO_000300: 2.140679e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.0579e1

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1053C>A
hgvsp: ENSP00000432851.1:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1044C>A
hgvsp: ENSP00000433844.1:p.His348Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1053C>A
hgvsp: ENSP00000434917.1:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*642C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1053C>A
hgvsp: ENSP00000413011.2:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1053C>A
hgvsp: ENSP00000356786.2:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1169C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1044C>A
hgvsp: ENSP00000434723.1:p.His348Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1053C>A
hgvsp: ENSP00000356788.4:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1392C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1053C>A
hgvsp: ENSP00000434639.1:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1053C>A
hgvsp: ENSP00000432811.1:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1044C>A
hgvsp: ENSP00000410825.2:p.His348Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.948C>A
hgvsp: ENSP00000436605.1:p.His316Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*122C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1053C>A
hgvsp: ENSP00000432877.1:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*122C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1053C>A
hgvsp: ENSP00000433745.1:p.His351Gln
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*122C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*122C>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13232
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2061
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16708
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5795
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1181
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3648
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8657
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21043
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3253
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14257
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.17e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.056e0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.140343e6

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*127C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1058C>A
hgvsp: ENSP00000434816.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1058C>A
hgvsp: ENSP00000341050.5:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1058C>A
hgvsp: ENSP00000356788.4:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1049C>A
hgvsp: ENSP00000434795.1:p.Ser350Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1174C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*127C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1058C>A
hgvsp: ENSP00000432948.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1049C>A
hgvsp: ENSP00000433458.1:p.Ser350Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1058C>A
hgvsp: ENSP00000434917.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*647C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1058C>A
hgvsp: ENSP00000435293.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*127C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*525C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+36G>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1058C>A
hgvsp: ENSP00000433227.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1058C>A
hgvsp: ENSP00000432168.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1058C>A
hgvsp: ENSP00000433745.1:p.Ser353Tyr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1397C>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1049C>A
hgvsp: ENSP00000433844.1:p.Ser350Tyr
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 260
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2061
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3646
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6552
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16708
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13223
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5794
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 744
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8654
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 572
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3248
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14250
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.211e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.591e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e-1

DP
type: SiteQuality
SIO_000300: 2.140062e6

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1064C>T
hgvsp: ENSP00000432877.1:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*133C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1180C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1064C>T
hgvsp: ENSP00000432811.1:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1064C>T
hgvsp: ENSP00000413011.2:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1055C>T
hgvsp: ENSP00000434723.1:p.Pro352Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1055C>T
hgvsp: ENSP00000434795.1:p.Pro352Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1064C>T
hgvsp: ENSP00000435055.1:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+30G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1064C>T
hgvsp: ENSP00000341050.5:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1064C>T
hgvsp: ENSP00000434420.1:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.116C>T
hgvsp: ENSP00000432042.1:p.Pro39Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1055C>T
hgvsp: ENSP00000433844.1:p.Pro352Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.959C>T
hgvsp: ENSP00000436605.1:p.Pro320Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*133C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*133C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*133C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1064C>T
hgvsp: ENSP00000432168.1:p.Pro355Leu
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*133C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*653C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 1181
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16722
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8645
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6562
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3643
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13214
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5788
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14245
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7271
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4965
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.081e0

QD
type: SiteQuality
SIO_000300: 1.228e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

DP
type: SiteQuality
SIO_000300: 2.139388e6

FS
type: SiteQuality
SIO_000300: 2.376e0

MQ
type: SiteQuality
SIO_000300: 5.921e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.139e0

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1076C>T
hgvsp: ENSP00000432877.1:p.Ala359Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*145C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*145C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1192C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1076C>T
hgvsp: ENSP00000339992.5:p.Ala359Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1076C>T
hgvsp: ENSP00000433745.1:p.Ala359Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1067C>T
hgvsp: ENSP00000434795.1:p.Ala356Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*145C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*665C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*543C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1415C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1076C>T
hgvsp: ENSP00000432811.1:p.Ala359Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*145C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*145C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+18G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1076C>T
hgvsp: ENSP00000356786.2:p.Ala359Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.971C>T
hgvsp: ENSP00000436605.1:p.Ala324Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1067C>T
hgvsp: ENSP00000433458.1:p.Ala356Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1067C>T
hgvsp: ENSP00000410825.2:p.Ala356Val
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1076C>T
hgvsp: ENSP00000435055.1:p.Ala359Val
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 8624
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13211
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6591
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3640
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1180
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2060
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16707
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5779
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21082
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4954
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14233
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

QD
type: SiteQuality
SIO_000300: 1.457e1

FS
type: SiteQuality
SIO_000300: 2.293e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 2.138432e6

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1077G>A
hgvsp: ENST00000528140.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1077G>A
hgvsp: ENST00000341911.5:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*146G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*146G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*146G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*146G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1077G>A
hgvsp: ENST00000339290.5:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.129G>A
hgvsp: ENST00000534736.1:c.129G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*666G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*544G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1077G>A
hgvsp: ENST00000531737.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+17C>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1077G>A
hgvsp: ENST00000533808.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1077G>A
hgvsp: ENST00000525002.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1077G>A
hgvsp: ENST00000528343.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1077G>A
hgvsp: ENST00000533837.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1077G>A
hgvsp: ENST00000525940.1:c.1077G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1068G>A
hgvsp: ENST00000528774.1:c.1068G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1416G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1416G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2058
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 308
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3633
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13206
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 569
bin: 6.75e1
variant carriers: 3

GenotypeDepth
all individuals: 5780
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 6.25e1
variant carriers: 5

GenotypeDepth
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16713
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6593
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 8623
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1184
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21094
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4947
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3380
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14234
bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 2142
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 30
allele frequency: 2.596053997923157e-3
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

DP
type: SiteQuality
SIO_000300: 2.138449e6

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

FS
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1083T>G
hgvsp: ENST00000534044.1:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1083T>G
hgvsp: ENST00000316528.8:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1083T>G
hgvsp: ENST00000339290.5:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1083T>G
hgvsp: ENST00000525002.1:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*550T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*152T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*152T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1422T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.978T>G
hgvsp: ENST00000533624.1:c.978T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.103+11A>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1083T>G
hgvsp: ENST00000528015.1:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1083T>G
hgvsp: ENST00000525940.1:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1199T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1083T>G
hgvsp: ENST00000438901.2:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1083T>G
hgvsp: ENST00000528343.1:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*152T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*152T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1422T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1074T>G
hgvsp: ENST00000528774.1:c.1074T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1083T>G
hgvsp: ENST00000533384.1:c.1083T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3637
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2053
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1177
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 735
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6615
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16741
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13200
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 403
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5765
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8602
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14213
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4954
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21111
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.934812760055479e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.792e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

QD
type: SiteQuality
SIO_000300: 1.301e1

DP
type: SiteQuality
SIO_000300: 2.136929e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1085G>A
hgvsp: ENSP00000432877.1:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*154G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1085G>A
hgvsp: ENSP00000435293.1:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.980G>A
hgvsp: ENSP00000436605.1:p.Gly327Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1085G>A
hgvsp: ENSP00000413011.2:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1085G>A
hgvsp: ENSP00000434816.1:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1076G>A
hgvsp: ENSP00000410825.2:p.Gly359Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1085G>A
hgvsp: ENSP00000434639.1:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1424G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1085G>A
hgvsp: ENSP00000341050.5:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*674G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*154G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*154G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1076G>A
hgvsp: ENSP00000434795.1:p.Gly359Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1085G>A
hgvsp: ENSP00000356786.2:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1085G>A
hgvsp: ENSP00000356788.4:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.137G>A
hgvsp: ENSP00000432042.1:p.Gly46Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1085G>A
hgvsp: ENSP00000434420.1:p.Gly362Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*154G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5762
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6623
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3637
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2052
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16740
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13198
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1174
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8597
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21109
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7266
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4948
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14203
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4153
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

MQ
type: SiteQuality
SIO_000300: 5.901e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.136067e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.024e0

VQSLOD
type: SiteQuality
SIO_000300: -2.677e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.188e0

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1104C>T
hgvsp: ENST00000525002.1:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1104C>T
hgvsp: ENST00000533808.1:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1104C>T
hgvsp: ENST00000525940.1:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1104C>T
hgvsp: ENST00000534121.1:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1104C>T
hgvsp: ENST00000367814.4:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1104C>T
hgvsp: ENST00000316528.8:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*173C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1220C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1104C>T
hgvsp: ENST00000339290.5:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1095C>T
hgvsp: ENST00000526889.1:c.1095C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*173C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1104C>T
hgvsp: ENST00000367812.2:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1095C>T
hgvsp: ENST00000442647.2:c.1095C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1104C>T
hgvsp: ENST00000438901.2:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*173C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1443C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*173C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*571C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1104C>T
hgvsp: ENST00000531737.1:c.1104C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*173C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13157
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3621
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5733
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16754
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1170
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 733
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6723
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2045
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8546
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21150
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4901
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3357
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.31e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

FS
type: SiteQuality
SIO_000300: 1.044e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.133254e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.148e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1105G>A
hgvsp: ENSP00000434917.1:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1105G>A
hgvsp: ENSP00000434420.1:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*174G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1105G>A
hgvsp: ENSP00000356786.2:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*174G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*174G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.92C>T
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1105G>A
hgvsp: ENSP00000341050.5:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.157G>A
hgvsp: ENSP00000432042.1:p.Ala53Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1105G>A
hgvsp: ENSP00000326328.8:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1096G>A
hgvsp: ENSP00000434795.1:p.Ala366Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1105G>A
hgvsp: ENSP00000432948.1:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.1000G>A
hgvsp: ENSP00000436605.1:p.Ala334Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1096G>A
hgvsp: ENSP00000434723.1:p.Ala366Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1105G>A
hgvsp: ENSP00000413011.2:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1105G>A
hgvsp: ENSP00000433745.1:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*572G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1444G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1105G>A
hgvsp: ENSP00000433227.1:p.Ala369Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1444G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 3616
bin: 4.75e1
variant carriers: 8

GenotypeDepth
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 733
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 259
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 569
bin: 6.75e1
variant carriers: 6

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8530
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16773
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5729
bin: 4.25e1
variant carriers: 5

GenotypeDepth
all individuals: 13144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1170
bin: 5.75e1
variant carriers: 4

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 2043
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 6732
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7229
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4905
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14188
bin: 9.75e1
variant carriers: 36

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 30
allele frequency: 2.596952908587258e-3
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.494678778067572e-5
allele num: 66714
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 2.133251e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*705A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1107A>G
hgvsp: ENST00000526889.1:c.1107A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1455A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1232A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*185A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1116A>G
hgvsp: ENST00000341911.5:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*583A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1116A>G
hgvsp: ENST00000534121.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1116A>G
hgvsp: ENST00000527615.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1116A>G
hgvsp: ENST00000339290.5:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1116A>G
hgvsp: ENST00000525002.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.81T>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1116A>G
hgvsp: ENST00000533837.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1116A>G
hgvsp: ENST00000533384.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1116A>G
hgvsp: ENST00000533808.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.1011A>G
hgvsp: ENST00000533624.1:c.1011A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1116A>G
hgvsp: ENST00000528343.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*185A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1116A>G
hgvsp: ENST00000534044.1:c.1116A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*185A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*185A>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13108
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3595
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5711
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2032
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 563
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6825
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8501
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16841
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1167
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3350
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4892
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.8e0

FS
type: SiteQuality
SIO_000300: 6.984e0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.523e1

DP
type: SiteQuality
SIO_000300: 2.130982e6

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+4C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1113C>T
hgvsp: ENST00000526889.1:c.1113C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.174C>T
hgvsp: ENST00000534736.1:c.174C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1122C>T
hgvsp: ENST00000438901.2:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1122C>T
hgvsp: ENST00000533837.1:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1122C>T
hgvsp: ENST00000533808.1:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1122C>T
hgvsp: ENST00000367812.2:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*191C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1122C>T
hgvsp: ENST00000533384.1:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1113C>T
hgvsp: ENST00000442647.2:c.1113C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*191C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1122C>T
hgvsp: ENST00000367814.4:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*711C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1122C>T
hgvsp: ENST00000316528.8:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*191C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1122C>T
hgvsp: ENST00000339290.5:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1113C>T
hgvsp: ENST00000528774.1:c.1113C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1461C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1122C>T
hgvsp: ENST00000528343.1:c.1122C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1238C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 16851
bin: 2.75e1
variant carriers: 5

GenotypeDepth
all individuals: 115
bin: 9.25e1
variant carriers: 8

GenotypeDepth
all individuals: 302
bin: 7.75e1
variant carriers: 14

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 6.75e1
variant carriers: 30

GenotypeDepth
all individuals: 6832
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 414
bin: 7.25e1
variant carriers: 30

GenotypeDepth
all individuals: 8479
bin: 3.75e1
variant carriers: 24

GenotypeDepth
all individuals: 250
bin: 8.25e1
variant carriers: 14

GenotypeDepth
all individuals: 159
bin: 8.75e1
variant carriers: 11

GenotypeDepth
all individuals: 3577
bin: 4.75e1
variant carriers: 30

GenotypeDepth
all individuals: 5686
bin: 4.25e1
variant carriers: 30

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13071
bin: 3.25e1
variant carriers: 13

GenotypeDepth
all individuals: 736
bin: 6.25e1
variant carriers: 27

GenotypeDepth
all individuals: 306
bin: 9.75e1
variant carriers: 62

GenotypeDepth
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1173
bin: 5.75e1
variant carriers: 42

GenotypeDepth
all individuals: 2032
bin: 5.25e1
variant carriers: 37

GenotypeQuality
all individuals: 21438
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4097
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4856
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14235
bin: 9.75e1
variant carriers: 380

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.471097265489789e-3
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995743022454058e-5
allele num: 66714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 366
allele frequency: 3.518554124206883e-2
allele num: 10402
num of homozygotes: 6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.137299e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.131e0

VQSLOD
type: SiteQuality
SIO_000300: 6.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.55e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.415e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+8A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+8A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1117A>T
hgvsp: ENSP00000433458.1:p.Ile373Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1126A>T
hgvsp: ENSP00000434420.1:p.Ile376Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*195A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1465A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1126A>T
hgvsp: ENSP00000432811.1:p.Ile376Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*195A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1126A>T
hgvsp: ENSP00000326328.8:p.Ile376Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*593A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.71T>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*195A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+8A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+8A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*195A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1465A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.178A>T
hgvsp: ENSP00000432042.1:p.Ile60Phe
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+8A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+8A>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*195A>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 8507
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3554
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6878
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13141
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16949
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1145
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5693
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2011
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3348
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4892
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4122
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.923e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.123957e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e0

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

FS
type: SiteQuality
SIO_000300: 8.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.963e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+10C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1119C>T
hgvsp: ENST00000528774.1:c.1119C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1128C>T
hgvsp: ENST00000528343.1:c.1128C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1128C>T
hgvsp: ENST00000534121.1:c.1128C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1128C>T
hgvsp: ENST00000533384.1:c.1128C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+10C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1244C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1467C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+10C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+10C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1128C>T
hgvsp: ENST00000534044.1:c.1128C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+10C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1128C>T
hgvsp: ENST00000367814.4:c.1128C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.69G>A
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1467C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1128C>T
hgvsp: ENST00000533837.1:c.1128C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*595C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*197C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*197C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+10C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2011
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6879
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5698
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 717
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 386
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13138
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8505
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3551
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16951
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4883
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13963
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 21606
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3147
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.494454103963068e-5
allele num: 66716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.482e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

QD
type: SiteQuality
SIO_000300: 1.505e1

DP
type: SiteQuality
SIO_000300: 2.124007e6

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1133A>G
hgvsp: ENSP00000434639.1:p.His378Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*202A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*202A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1124A>G
hgvsp: ENSP00000433458.1:p.His375Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1472A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*722A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1124A>G
hgvsp: ENSP00000434723.1:p.His375Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1133A>G
hgvsp: ENSP00000326328.8:p.His378Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1133A>G
hgvsp: ENSP00000435055.1:p.His378Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1472A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1133A>G
hgvsp: ENSP00000432811.1:p.His378Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*202A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+15A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1133A>G
hgvsp: ENSP00000413011.2:p.His378Arg
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+15A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.64T>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+15A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+15A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+15A>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1249A>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 716
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5687
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6910
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8499
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2010
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3550
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16970
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13117
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21654
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3348
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4880
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13951
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.944e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.123297e6

FS
type: SiteQuality
SIO_000300: 4.912e0

VQSLOD
type: SiteQuality
SIO_000300: -2.334e0

MQ
type: SiteQuality
SIO_000300: 5.568e1

MQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.439e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+21G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1139G>A
hgvsp: ENSP00000434639.1:p.Gly380Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1130G>A
hgvsp: ENSP00000434723.1:p.Gly377Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1139G>A
hgvsp: ENSP00000433745.1:p.Gly380Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1139G>A
hgvsp: ENSP00000339992.5:p.Gly380Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*606G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*208G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*208G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*208G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+21G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+21G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+21G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1139G>A
hgvsp: ENSP00000433227.1:p.Gly380Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1478G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+21G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+21G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1139G>A
hgvsp: ENSP00000356788.4:p.Gly380Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1130G>A
hgvsp: ENSP00000433458.1:p.Gly377Asp
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1478G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 386
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3551
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5684
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8493
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6934
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2008
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13082
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16982
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13950
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3344
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21699
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3136
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7223
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.84e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.122685e6

FS
type: SiteQuality
SIO_000300: 2.821e0

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.532e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1155T>C
hgvsp: ENST00000339290.5:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1155T>C
hgvsp: ENST00000533384.1:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155T>C
hgvsp: ENST00000534121.1:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*622T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*224T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1155T>C
hgvsp: ENST00000367812.2:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1271T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1155T>C
hgvsp: ENST00000534044.1:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.1050T>C
hgvsp: ENST00000533624.1:c.1050T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*224T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1155T>C
hgvsp: ENST00000528343.1:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1494T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+37T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1155T>C
hgvsp: ENST00000316528.8:c.1155T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16975
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8473
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3544
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13032
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2006
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7003
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5677
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13944
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7190
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4838
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.514e0

DP
type: SiteQuality
SIO_000300: 2.121199e6

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.76e-1

FS
type: SiteQuality
SIO_000300: 1.3876e1

VQSLOD
type: SiteQuality
SIO_000300: -2.395e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1160A>C
hgvsp: ENSP00000435293.1:p.Lys387Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1160A>C
hgvsp: ENSP00000356786.2:p.Lys387Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155+5A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+42A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.212A>C
hgvsp: ENSP00000432042.1:p.Lys71Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+5A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1499A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+42A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.37T>G
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*627A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*229A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1160A>C
hgvsp: ENSP00000356788.4:p.Lys387Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*749A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+42A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*229A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1160A>C
hgvsp: ENSP00000432811.1:p.Lys387Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+42A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1160A>C
hgvsp: ENSP00000434639.1:p.Lys387Thr
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+42A>C
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 3541
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13007
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7014
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16979
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5676
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8469
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2006
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13943
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4832
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7154
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3113
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.120578e6

VQSLOD
type: SiteQuality
SIO_000300: -1.696e0

QD
type: SiteQuality
SIO_000300: 1.306e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.584e0

FS
type: SiteQuality
SIO_000300: 1.876e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.951e0

MQ
type: SiteQuality
SIO_000300: 5.646e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1532T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1193T>G
hgvsp: ENSP00000339992.5:p.Phe398Cys
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*262T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+75T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000118513
ensembl transcript: ENST00000531845
gene symbol: MYB
hgvsc: ENST00000531845.1:n.1309T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1193T>G
hgvsp: ENSP00000326328.8:p.Phe398Cys
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*660T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*262T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+75T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000236703
ensembl transcript: ENST00000455534
gene symbol: MYB-AS1
hgvsc: ENST00000455534.1:n.4A>C
variant of: http://identifiers.org/hgnc/37457

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+75T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+75T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1193T>G
hgvsp: ENSP00000435055.1:p.Phe398Cys
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1193T>G
hgvsp: ENSP00000434639.1:p.Phe398Cys
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1184T>G
hgvsp: ENSP00000410825.2:p.Phe395Cys
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*782T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+75T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+38T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+75T>G
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1532T>G
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 262
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12861
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1144
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5665
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16835
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8409
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3540
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2005
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7052
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13935
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 21694
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4080
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7042
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00507858280494e-5
allele num: 66554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

QD
type: SiteQuality
SIO_000300: 1.254e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 1.574e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

DP
type: SiteQuality
SIO_000300: 2.113661e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*789T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*269T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+82T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+82T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1200T>C
hgvsp: ENST00000533837.1:c.1200T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*269T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1200T>C
hgvsp: ENST00000533808.1:c.1200T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155+45T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+45T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1200T>C
hgvsp: ENST00000367814.4:c.1200T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1191T>C
hgvsp: ENST00000442647.2:c.1191T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1191T>C
hgvsp: ENST00000526889.1:c.1191T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+82T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+82T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+82T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*667T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+82T>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*269T>C
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16740
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8402
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7031
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2005
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3538
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12807
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5662
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2092
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13932
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21566
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e0

FS
type: SiteQuality
SIO_000300: 3.42e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 2.110452e6

QD
type: SiteQuality
SIO_000300: 1.516e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e0

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.391e0

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.1098+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*670+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+92A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+92A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356786
ensembl transcript: ENST00000367812
gene symbol: MYB
hgvsc: ENST00000367812.2:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+55A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1549A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1203+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+92A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*792+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*272+7A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+92A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155+55A>C
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1194+7A>C
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 6895
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3540
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16442
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2005
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12694
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8387
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5661
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 711
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4753
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13933
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6925
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.65e0

VQSLOD
type: SiteQuality
SIO_000300: -2.371e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.539e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.643e0

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

DP
type: SiteQuality
SIO_000300: 2.101796e6

MQ
type: SiteQuality
SIO_000300: 5.875e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1203+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+105G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+68G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1203+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*670+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.255+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*272+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+105G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1562G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*792+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+105G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155+68G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+105G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1203+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1203+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1203+20G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1194+20G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 2005
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15849
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1633
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 601
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8350
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 524
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12470
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6225
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3540
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4038
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3318
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13925
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19873
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6627
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.881e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.0814e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

FS
type: SiteQuality
SIO_000300: 4.234e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+108G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1203+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1203+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1565G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+71G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434639
ensembl transcript: ENST00000533837
gene symbol: MYB
hgvsc: ENST00000533837.1:c.1203+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1194+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+108G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*272+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1565G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435293
ensembl transcript: ENST00000533808
gene symbol: MYB
hgvsc: ENST00000533808.1:c.1203+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+108G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000410825
ensembl transcript: ENST00000442647
gene symbol: MYB
hgvsc: ENST00000442647.2:c.1194+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000326328
ensembl transcript: ENST00000316528
gene symbol: MYB
hgvsc: ENST00000316528.8:c.1203+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*792+23G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+108G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1203+23G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15622
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2006
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8329
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 12403
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6060
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 779
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1896
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3540
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6588
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4033
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13924
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66194
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.937783922575548e-4
allele num: 10126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.715e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.143e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 3.686e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 2.075177e6

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.255+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433844
ensembl transcript: ENST00000529262
gene symbol: MYB
hgvsc: ENST00000529262.1:c.1109+113C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435055
ensembl transcript: ENST00000534044
gene symbol: MYB
hgvsc: ENST00000534044.1:c.1203+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*670+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*272+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*792+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000413011
ensembl transcript: ENST00000438901
gene symbol: MYB
hgvsc: ENST00000438901.2:c.1155+76C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434723
ensembl transcript: ENST00000528774
gene symbol: MYB
hgvsc: ENST00000528774.1:c.1194+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+113C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1570C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1194+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000339992
ensembl transcript: ENST00000341911
gene symbol: MYB
hgvsc: ENST00000341911.5:c.1203+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434917
ensembl transcript: ENST00000526320
gene symbol: MYB
hgvsc: ENST00000526320.1:c.1118+113C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*272+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433227
ensembl transcript: ENST00000527615
gene symbol: MYB
hgvsc: ENST00000527615.1:c.1203+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1203+28C>T
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155+76C>T
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 1498
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5471
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3538
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1142
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12189
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2004
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14913
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5640
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8285
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6360
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13917
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66086
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

DP
type: SiteQuality
SIO_000300: 2.056015e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 7.888e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

QD
type: SiteQuality
SIO_000300: 1.26e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.255+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436385
ensembl transcript: ENST00000526565
gene symbol: MYB
hgvsc: ENST00000526565.1:c.*272+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*272+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1194+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+114delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432877
ensembl transcript: ENST00000528140
gene symbol: MYB
hgvsc: ENST00000528140.1:c.1118+114delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1203+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*272+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*792+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1571delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000341050
ensembl transcript: ENST00000339290
gene symbol: MYB
hgvsc: ENST00000339290.5:c.1203+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435578
ensembl transcript: ENST00000525514
gene symbol: MYB
hgvsc: ENST00000525514.1:c.*272+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434420
ensembl transcript: ENST00000528343
gene symbol: MYB
hgvsc: ENST00000528343.1:c.1203+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435595
ensembl transcript: ENST00000531519
gene symbol: MYB
hgvsc: ENST00000531519.1:c.948+1571delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432851
ensembl transcript: ENST00000534121
gene symbol: MYB
hgvsc: ENST00000534121.1:c.1155+77delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*272+29delG
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+114delG
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12189
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5471
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3538
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14913
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8285
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1498
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5640
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1142
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2004
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6360
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13917
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 7.888e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

QD
type: SiteQuality
SIO_000300: 1.26e1

DP
type: SiteQuality
SIO_000300: 2.056015e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436925
ensembl transcript: ENST00000531634
gene symbol: MYB
hgvsc: ENST00000531634.1:c.*792+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434795
ensembl transcript: ENST00000526187
gene symbol: MYB
hgvsc: ENST00000526187.1:c.1109+114G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436605
ensembl transcript: ENST00000533624
gene symbol: MYB
hgvsc: ENST00000533624.1:c.1098+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435497
ensembl transcript: ENST00000528345
gene symbol: MYB
hgvsc: ENST00000528345.1:c.*272+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433458
ensembl transcript: ENST00000526889
gene symbol: MYB
hgvsc: ENST00000526889.1:c.1194+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000435938
ensembl transcript: ENST00000525369
gene symbol: MYB
hgvsc: ENST00000525369.1:c.948+1571G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432948
ensembl transcript: ENST00000525940
gene symbol: MYB
hgvsc: ENST00000525940.1:c.1118+114G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432811
ensembl transcript: ENST00000533384
gene symbol: MYB
hgvsc: ENST00000533384.1:c.1203+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000356788
ensembl transcript: ENST00000367814
gene symbol: MYB
hgvsc: ENST00000367814.4:c.1203+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434816
ensembl transcript: ENST00000528015
gene symbol: MYB
hgvsc: ENST00000528015.1:c.1118+114G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000434675
ensembl transcript: ENST00000524588
gene symbol: MYB
hgvsc: ENST00000524588.1:c.*670+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432042
ensembl transcript: ENST00000534736
gene symbol: MYB
hgvsc: ENST00000534736.1:c.255+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437264
ensembl transcript: ENST00000529586
gene symbol: MYB
hgvsc: ENST00000529586.1:c.*187+114G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000436602
ensembl transcript: ENST00000463282
gene symbol: MYB
hgvsc: ENST00000463282.2:c.*272+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000432168
ensembl transcript: ENST00000531737
gene symbol: MYB
hgvsc: ENST00000531737.1:c.1118+114G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000437081
ensembl transcript: ENST00000525477
gene symbol: MYB
hgvsc: ENST00000525477.1:c.*272+29G>A
variant of: http://identifiers.org/hgnc/7545

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000118513
ensembl protein: ENSP00000433745
ensembl transcript: ENST00000525002
gene symbol: MYB
hgvsc: ENST00000525002.1:c.1203+29G>A
variant of: http://identifiers.org/hgnc/7545

GenotypeDepth
all individuals: 2413
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14307
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3082
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11891
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5053
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8224
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5626
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3535
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2003
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 9.75e1
variant carriers: 0