9-36589546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589546
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589546
    reference: chr 9
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-548G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.307G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.158G>A
  hgvsp: ENSP00000298048.2:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.62G>A
  hgvsp: ENSP00000441596.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.158G>A
  hgvsp: ENSP00000437804.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.385G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.307G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.158G>A
  hgvsp: ENSP00000445452.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.158G>A
  hgvsp: ENSP00000439792.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-92G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5079G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg53Gln
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/9-36589550-CAAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589550
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589546
    reference: chr 9
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.312_315delAAAA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.67_70delAAAA
  hgvsp: ENSP00000441596.1:p.Lys23ArgfsTer6
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.163_166delAAAA
  hgvsp: ENSP00000437804.1:p.Lys55ArgfsTer6
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.390_393delAAAA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.163_166delAAAA
  hgvsp: ENSP00000445452.1:p.Lys55ArgfsTer6
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5074_49-5071delAAAA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.163_166delAAAA
  hgvsp: ENSP00000439792.1:p.Lys55ArgfsTer6
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-87_-84delAAAA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-543_-540delAAAA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.163_166delAAAA
  hgvsp: ENSP00000298048.2:p.Lys55ArgfsTer6
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.312_315delAAAA
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys55ArgfsTer6
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: CAAAA
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

9-36589554-A-AGTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589554
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589558
    reference: chr 9
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: AGTTT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.166_167insGTTT
  hgvsp: ENSP00000298048.2:p.Thr56SerfsTer5
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.166_167insGTTT
  hgvsp: ENSP00000439792.1:p.Thr56SerfsTer5
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.315_316insGTTT
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.393_394insGTTT
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.70_71insGTTT
  hgvsp: ENSP00000441596.1:p.Thr24SerfsTer5
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.166_167insGTTT
  hgvsp: ENSP00000445452.1:p.Thr56SerfsTer5
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.166_167insGTTT
  hgvsp: ENSP00000437804.1:p.Thr56SerfsTer5
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-540_-539insGTTT
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-84_-83insGTTT
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.315_316insGTTT
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5071_49-5070insGTTT
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 7628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr56SerfsTer5
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-36589555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589555
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589555
    reference: chr 9
allele count: 165
allele frequency: 1.359277688074604e-3
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.316C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5070C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.71C>T
  hgvsp: ENSP00000441596.1:p.Thr24Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.167C>T
  hgvsp: ENSP00000298048.2:p.Thr56Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-83C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.167C>T
  hgvsp: ENSP00000437804.1:p.Thr56Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.394C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.167C>T
  hgvsp: ENSP00000439792.1:p.Thr56Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.167C>T
  hgvsp: ENSP00000445452.1:p.Thr56Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-539C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.316C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 9.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Thr56Met
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

9-36589556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589556
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589556
    reference: chr 9
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-538G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.168G>A
  hgvsp: ENST00000298048.2:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-82G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.168G>A
  hgvsp: ENST00000541717.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.395G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.168G>A
  hgvsp: ENST00000536860.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5069G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.317G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.72G>A
  hgvsp: ENST00000543751.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.168G>A
  hgvsp: ENST00000545008.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.317G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr56Thr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

9-36589576-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589576
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589576
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5049A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.337A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.188A>G
  hgvsp: ENSP00000437804.1:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-518A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.92A>G
  hgvsp: ENSP00000441596.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.188A>G
  hgvsp: ENSP00000445452.1:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-62A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.188A>G
  hgvsp: ENSP00000439792.1:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.415A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.188A>G
  hgvsp: ENSP00000298048.2:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.337A>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn63Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-36589577-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589577
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589577
    reference: chr 9
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-61C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.416C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.189C>A
  hgvsp: ENSP00000437804.1:p.Asn63Lys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-517C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.93C>A
  hgvsp: ENSP00000441596.1:p.Asn31Lys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.189C>A
  hgvsp: ENSP00000445452.1:p.Asn63Lys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5048C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.189C>A
  hgvsp: ENSP00000439792.1:p.Asn63Lys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.338C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.189C>A
  hgvsp: ENSP00000298048.2:p.Asn63Lys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.338C>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn63Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-36589577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589577
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589577
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.189C>T
  hgvsp: ENST00000536860.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-61C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.189C>T
  hgvsp: ENST00000298048.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.93C>T
  hgvsp: ENST00000543751.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.189C>T
  hgvsp: ENST00000541717.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.189C>T
  hgvsp: ENST00000545008.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5048C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.338C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.416C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-517C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.338C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn63Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

9-36589578-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589578
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589578
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.94C>G
  hgvsp: ENSP00000441596.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.339C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.417C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.190C>G
  hgvsp: ENSP00000439792.1:p.Leu64Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.339C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.190C>G
  hgvsp: ENSP00000298048.2:p.Leu64Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.190C>G
  hgvsp: ENSP00000445452.1:p.Leu64Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.190C>G
  hgvsp: ENSP00000437804.1:p.Leu64Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-516C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5047C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-60C>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu64Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

9-36589579-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589579
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589579
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5046T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-515T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.191T>C
  hgvsp: ENSP00000439792.1:p.Leu64Pro
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.340T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.191T>C
  hgvsp: ENSP00000437804.1:p.Leu64Pro
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.95T>C
  hgvsp: ENSP00000441596.1:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.191T>C
  hgvsp: ENSP00000298048.2:p.Leu64Pro
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.191T>C
  hgvsp: ENSP00000445452.1:p.Leu64Pro
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.340T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.418T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu64Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/9-36589587-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589587
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589588
    reference: chr 9
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.200dupA
  hgvsp: ENSP00000445452.1:p.His68AlafsTer20
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5037dupA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.200dupA
  hgvsp: ENSP00000439792.1:p.His68AlafsTer20
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.200dupA
  hgvsp: ENSP00000298048.2:p.His68AlafsTer20
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-50dupA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-506dupA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.200dupA
  hgvsp: ENSP00000437804.1:p.His68AlafsTer20
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.104dupA
  hgvsp: ENSP00000441596.1:p.His36AlafsTer20
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.349dupA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.349dupA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.427dupA
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His68AlafsTer20
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

9-36589590-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589590
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589590
    reference: chr 9
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.106C>G
  hgvsp: ENSP00000441596.1:p.His36Asp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.202C>G
  hgvsp: ENSP00000298048.2:p.His68Asp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-504C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-48C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5035C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.202C>G
  hgvsp: ENSP00000445452.1:p.His68Asp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.351C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.202C>G
  hgvsp: ENSP00000437804.1:p.His68Asp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.429C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.202C>G
  hgvsp: ENSP00000439792.1:p.His68Asp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.351C>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His68Asp
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

9-36589593-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589593
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589593
    reference: chr 9
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5032A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.205A>T
  hgvsp: ENSP00000437804.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.432A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.354A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.205A>T
  hgvsp: ENSP00000298048.2:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-501A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.109A>T
  hgvsp: ENSP00000441596.1:p.Ile37Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.205A>T
  hgvsp: ENSP00000439792.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.205A>T
  hgvsp: ENSP00000445452.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.354A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-45A>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile69Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

9-36589610-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589610
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589610
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.371T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.449T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.222T>C
  hgvsp: ENST00000541717.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.222T>C
  hgvsp: ENST00000298048.2:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.222T>C
  hgvsp: ENST00000536860.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-484T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5015T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.126T>C
  hgvsp: ENST00000543751.1:c.126T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.371T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.222T>C
  hgvsp: ENST00000545008.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His74His
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

9-36589611-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589611
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589611
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-483G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.223G>A
  hgvsp: ENSP00000445452.1:p.Val75Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.372G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.372G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-27G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.450G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.223G>A
  hgvsp: ENSP00000439792.1:p.Val75Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.223G>A
  hgvsp: ENSP00000298048.2:p.Val75Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.127G>A
  hgvsp: ENSP00000441596.1:p.Val43Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5014G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.223G>A
  hgvsp: ENSP00000437804.1:p.Val75Met
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val75Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

9-36589612-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589612
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589612
    reference: chr 9
allele count: 9
allele frequency: 7.413509060955519e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.373T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-26T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.451T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5013T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.224T>G
  hgvsp: ENSP00000437804.1:p.Val75Gly
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.373T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.224T>G
  hgvsp: ENSP00000439792.1:p.Val75Gly
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.224T>G
  hgvsp: ENSP00000445452.1:p.Val75Gly
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.128T>G
  hgvsp: ENSP00000441596.1:p.Val43Gly
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.224T>G
  hgvsp: ENSP00000298048.2:p.Val75Gly
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-482T>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val75Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

9-36589616-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589616
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589616
    reference: chr 9
allele count: 60
allele frequency: 4.942583653228331e-4
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.132A>G
  hgvsp: ENST00000543751.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.377A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-478A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.228A>G
  hgvsp: ENST00000536860.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.228A>G
  hgvsp: ENST00000541717.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.455A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5009A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.228A>G
  hgvsp: ENST00000545008.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.377A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.228A>G
  hgvsp: ENST00000298048.2:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11130
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Leu76Leu
num of homozygotes: 1
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-36589617-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589617
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589617
    reference: chr 9
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.133G>T
  hgvsp: ENSP00000441596.1:p.Glu45Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.229G>T
  hgvsp: ENSP00000439792.1:p.Glu77Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.229G>T
  hgvsp: ENSP00000298048.2:p.Glu77Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5008G>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.378G>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.229G>T
  hgvsp: ENSP00000437804.1:p.Glu77Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.229G>T
  hgvsp: ENSP00000445452.1:p.Glu77Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.456G>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-21G>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-477G>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.378G>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu77Ter
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

9-36589621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589621
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589621
    reference: chr 9
allele count: 5
allele frequency: 4.119091163725636e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.137C>T
  hgvsp: ENSP00000441596.1:p.Thr46Ile
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.382C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-5004C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.233C>T
  hgvsp: ENSP00000298048.2:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.233C>T
  hgvsp: ENSP00000439792.1:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.382C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.233C>T
  hgvsp: ENSP00000437804.1:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.233C>T
  hgvsp: ENSP00000445452.1:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-473C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.460C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr78Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-36589638-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589638
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589638
    reference: chr 9
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.250A>T
  hgvsp: ENSP00000437804.1:p.Met84Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.399A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.1A>T
  hgvsp: ENSP00000439184.1:p.Met1?
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.250A>T
  hgvsp: ENSP00000445452.1:p.Met84Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.250A>T
  hgvsp: ENSP00000298048.2:p.Met84Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-456A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.399A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.154A>T
  hgvsp: ENSP00000441596.1:p.Met52Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.250A>T
  hgvsp: ENSP00000439792.1:p.Met84Leu
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.477A>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-4987A>T
  variant of: http://identifiers.org/hgnc/16870
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS

9-36589652-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589652
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589652
    reference: chr 9
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.165+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-445+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-4973T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.410+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.12+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.261+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.410+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.261+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.488+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.261+3T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.261+3T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.261+3T>C
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

9-36589652-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589652
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589652
    reference: chr 9
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.12+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.261+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.410+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-4973T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.165+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-445+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.261+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.488+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.261+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.261+3T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.410+3T>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.261+3T>G
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-36589660-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589660
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589660
    reference: chr 9
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.261+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.12+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.261+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.410+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-4965T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.165+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-445+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.261+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.410+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.488+11T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.261+11T>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

9-36589672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589672
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589672
    reference: chr 9
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.12+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.261+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.410+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.261+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.410+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.261+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.165+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.261+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-4953C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.488+23C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-445+23C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

9-36589697-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36589697
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36589697
    reference: chr 9
allele count: 3
allele frequency: 2.485789569626966e-5
allele num: 120686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.410+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.261+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-4928A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-445+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.165+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.261+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.488+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.261+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.12+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.410+48A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.261+48A>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9198
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4324
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

9-36594589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594589
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594589
    reference: chr 9
allele count: 3
allele frequency: 2.490618669677548e-5
allele num: 120452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-36G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.262-36G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.166-36G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4802G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.262-36G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.489-36G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2630G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-444-36G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2630G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2630G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4802G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4291
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

9-36594598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594598
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594598
    reference: chr 9
allele count: 2
allele frequency: 1.657742486282181e-5
allele num: 120646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2621A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4793A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-27A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.262-27A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.489-27A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2621A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2621A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-444-27A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4793A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.262-27A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.166-27A>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/9-36594607-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594607
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594607
    reference: chr 9
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.489-18A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-18A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.166-18A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.262-18A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2612A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.262-18A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4784A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2612A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4784A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2612A>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-444-18A>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-36594607-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594607
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594607
    reference: chr 9
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.489-18A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2612A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.262-18A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4784A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.166-18A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2612A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4784A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2612A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-444-18A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.262-18A>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

9-36594611-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594611
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594611
    reference: chr 9
allele count: 2
allele frequency: 1.653357141676174e-5
allele num: 120966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2608C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.262-14C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4780C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-14C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-444-14C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.489-14C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4780C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2608C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.262-14C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2608C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.166-14C>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

9-36594617-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594617
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594617
    reference: chr 9
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.166-8T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4774T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.262-8T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2602T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.489-8T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2602T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-444-8T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.262-8T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2602T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.49-8T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4774T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.262-8T>C
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-36594627-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594627
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594627
    reference: chr 9
allele count: 5
allele frequency: 4.125208323020312e-5
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.264C>T
  hgvsp: ENST00000541717.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.264C>T
  hgvsp: ENST00000298048.2:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.168C>T
  hgvsp: ENST00000543751.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.51C>T
  hgvsp: ENST00000536329.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2592C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4764C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2592C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4764C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2592C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.491C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-442C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.264C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

9-36594639-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594639
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594639
    reference: chr 9
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-430A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2580A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.276A>G
  hgvsp: ENST00000298048.2:c.276A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2580A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.276A>G
  hgvsp: ENST00000541717.1:c.276A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.503A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.180A>G
  hgvsp: ENST00000543751.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.63A>G
  hgvsp: ENST00000536329.1:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4752A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4752A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2580A>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly92Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

9-36594643-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594643
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594643
    reference: chr 9
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2576C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.67C>T
  hgvsp: ENST00000536329.1:c.67C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4748C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.280C>T
  hgvsp: ENST00000541717.1:c.280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.184C>T
  hgvsp: ENST00000543751.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2576C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2576C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-426C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.280C>T
  hgvsp: ENST00000298048.2:c.280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4748C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.507C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu94Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

9-36594651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594651
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594651
    reference: chr 9
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2568C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.288C>T
  hgvsp: ENST00000541717.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2568C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.288C>T
  hgvsp: ENST00000298048.2:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-418C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.75C>T
  hgvsp: ENST00000536329.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.515C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.192C>T
  hgvsp: ENST00000543751.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2568C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4740C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4740C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp96Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

9-36594654-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594654
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594654
    reference: chr 9
allele count: 8
allele frequency: 6.590111537637774e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.518T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4737T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.291T>C
  hgvsp: ENST00000298048.2:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2565T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4737T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.78T>C
  hgvsp: ENST00000536329.1:c.78T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2565T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2565T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.195T>C
  hgvsp: ENST00000543751.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.291T>C
  hgvsp: ENST00000541717.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-415T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr97Tyr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS

9-36594655-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594655
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594655
    reference: chr 9
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2564A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.292A>G
  hgvsp: ENSP00000437804.1:p.Ile98Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.292A>G
  hgvsp: ENSP00000298048.2:p.Ile98Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.519A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4736A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4736A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.79A>G
  hgvsp: ENSP00000443550.1:p.Ile27Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2564A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-414A>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.196A>G
  hgvsp: ENSP00000441596.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2564A>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile98Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

9-36594664-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594664
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594664
    reference: chr 9
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.205C>T
  hgvsp: ENSP00000441596.1:p.Gln69Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2555C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.301C>T
  hgvsp: ENSP00000437804.1:p.Gln101Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.301C>T
  hgvsp: ENSP00000298048.2:p.Gln101Ter
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.528C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4727C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2555C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-405C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2555C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4727C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.88C>T
  hgvsp: ENSP00000443550.1:p.Gln30Ter
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln101Ter
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

9-36594671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594671
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594671
    reference: chr 9
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.212G>A
  hgvsp: ENSP00000441596.1:p.Arg71His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.308G>A
  hgvsp: ENSP00000298048.2:p.Arg103His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.308G>A
  hgvsp: ENSP00000437804.1:p.Arg103His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.95G>A
  hgvsp: ENSP00000443550.1:p.Arg32His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2548G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4720G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4720G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-398G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.535G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2548G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2548G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg103His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

9-36594682-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594682
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594682
    reference: chr 9
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.319G>C
  hgvsp: ENSP00000298048.2:p.Glu107Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.319G>C
  hgvsp: ENSP00000437804.1:p.Glu107Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.223G>C
  hgvsp: ENSP00000441596.1:p.Glu75Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2537G>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4709G>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.106G>C
  hgvsp: ENSP00000443550.1:p.Glu36Gln
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2537G>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2537G>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-387G>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.546G>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4709G>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu107Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

9-36594691-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594691
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594691
    reference: chr 9
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4700C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-378C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.115C>T
  hgvsp: ENSP00000443550.1:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.232C>T
  hgvsp: ENSP00000441596.1:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.328C>T
  hgvsp: ENSP00000298048.2:p.Arg110Trp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.328C>T
  hgvsp: ENSP00000437804.1:p.Arg110Trp
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2528C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2528C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.555C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2528C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4700C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg110Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

9-36594695-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594695
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594695
    reference: chr 9
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4696T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.332T>C
  hgvsp: ENSP00000437804.1:p.Val111Ala
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2524T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.119T>C
  hgvsp: ENSP00000443550.1:p.Val40Ala
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.236T>C
  hgvsp: ENSP00000441596.1:p.Val79Ala
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2524T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.559T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4696T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.332T>C
  hgvsp: ENSP00000298048.2:p.Val111Ala
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-374T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2524T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val111Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

9-36594703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594703
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594703
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.244C>T
  hgvsp: ENSP00000441596.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-366C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.340C>T
  hgvsp: ENSP00000437804.1:p.Arg114Cys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2516C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4688C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2516C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4688C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.127C>T
  hgvsp: ENSP00000443550.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.340C>T
  hgvsp: ENSP00000298048.2:p.Arg114Cys
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.567C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2516C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg114Cys
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

9-36594704-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594704
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594704
    reference: chr 9
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.245G>A
  hgvsp: ENSP00000441596.1:p.Arg82His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2515G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-365G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4687G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2515G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.341G>A
  hgvsp: ENSP00000437804.1:p.Arg114His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4687G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.341G>A
  hgvsp: ENSP00000298048.2:p.Arg114His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.128G>A
  hgvsp: ENSP00000443550.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.568G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2515G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg114His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

9-36594729-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594729
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594729
    reference: chr 9
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.366T>C
  hgvsp: ENST00000298048.2:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4662T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2490T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.270T>C
  hgvsp: ENST00000543751.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.153T>C
  hgvsp: ENST00000536329.1:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4662T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.593T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.366T>C
  hgvsp: ENST00000541717.1:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-340T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2490T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2490T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr122Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

9-36594730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594730
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594730
    reference: chr 9
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2489G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2489G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2489G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.154G>A
  hgvsp: ENSP00000443550.1:p.Val52Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.271G>A
  hgvsp: ENSP00000441596.1:p.Val91Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.367G>A
  hgvsp: ENSP00000437804.1:p.Val123Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-339G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4661G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.367G>A
  hgvsp: ENSP00000298048.2:p.Val123Met
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.594G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4661G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val123Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

9-36594735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594735
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594735
    reference: chr 9
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.372C>T
  hgvsp: ENST00000541717.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-334C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.372C>T
  hgvsp: ENST00000298048.2:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2484C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.159C>T
  hgvsp: ENST00000536329.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.276C>T
  hgvsp: ENST00000543751.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.599C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2484C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4656C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4656C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2484C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His124His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

9-36594738-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594738
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594738
    reference: chr 9
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2481C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2481C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.279C>G
  hgvsp: ENSP00000441596.1:p.Ser93Arg
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.602C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-331C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.162C>G
  hgvsp: ENSP00000443550.1:p.Ser54Arg
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4653C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2481C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.375C>G
  hgvsp: ENSP00000298048.2:p.Ser125Arg
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4653C>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.375C>G
  hgvsp: ENSP00000437804.1:p.Ser125Arg
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser125Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-36594751-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594751
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594751
    reference: chr 9
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.615C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2468C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.388C>T
  hgvsp: ENSP00000298048.2:p.His130Tyr
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.292C>T
  hgvsp: ENSP00000441596.1:p.His98Tyr
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2468C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4640C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-318C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.388C>T
  hgvsp: ENSP00000437804.1:p.His130Tyr
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2468C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.175C>T
  hgvsp: ENSP00000443550.1:p.His59Tyr
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4640C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His130Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

9-36594757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594757
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594757
    reference: chr 9
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2462G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.298G>A
  hgvsp: ENSP00000441596.1:p.Asp100Asn
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4634G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.621G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-312G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2462G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.394G>A
  hgvsp: ENSP00000437804.1:p.Asp132Asn
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.394G>A
  hgvsp: ENSP00000298048.2:p.Asp132Asn
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2462G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4634G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.181G>A
  hgvsp: ENSP00000443550.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp132Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

9-36594761-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594761
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594761
    reference: chr 9
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2458T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.185T>A
  hgvsp: ENSP00000443550.1:p.Leu62His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.398T>A
  hgvsp: ENSP00000437804.1:p.Leu133His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.302T>A
  hgvsp: ENSP00000441596.1:p.Leu101His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2458T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4630T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4630T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-308T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2458T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.398T>A
  hgvsp: ENSP00000298048.2:p.Leu133His
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.625T>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu133His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/9-36594762-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594762
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594762
    reference: chr 9
allele count: 492
allele frequency: 4.131606791958483e-3
allele num: 119082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.303C>A
  hgvsp: ENST00000543751.1:c.303C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.399C>A
  hgvsp: ENST00000298048.2:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2457C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4629C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.399C>A
  hgvsp: ENST00000541717.1:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2457C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4629C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-307C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.186C>A
  hgvsp: ENST00000536329.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2457C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.626C>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6221
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10208
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 5.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9033
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 9.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 6.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
hgvs: p.Leu133Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD

9-36594774-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594774
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594774
    reference: chr 9
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+6T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2445T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+6T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+6T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4617T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2445T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+6T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2445T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+6T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4617T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+6T>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.405+6T>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

9-36594775-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594775
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594774
    reference: chr 9
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+8delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+8delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+8delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+8delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2443delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2443delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2443delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+8delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4615delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+8delA
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4615delA
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.405+8delA
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: GA
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum

9-36594783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594783
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594783
    reference: chr 9
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+15C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4608C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+15C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2436C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+15C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4608C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2436C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+15C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+15C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2436C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+15C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19458
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

9-36594789-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594789
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594789
    reference: chr 9
allele count: 20
allele frequency: 1.654670306941342e-4
allele num: 120870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2430T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2430T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4602T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+21T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4602T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+21T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+21T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+21T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+21T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2430T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+21T>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

9-36594795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594795
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594795
    reference: chr 9
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4596C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+27C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+27C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4596C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+27C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2424C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2424C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+27C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+27C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+27C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2424C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-36594797-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594797
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594797
    reference: chr 9
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4594C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4594C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+29C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+29C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+29C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+29C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2422C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+29C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2422C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+29C>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2422C>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

9-36594797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594797
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594797
    reference: chr 9
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+29C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4594C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2422C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2422C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+29C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2422C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+29C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+29C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+29C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+29C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4594C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

9-36594799-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594799
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594799
    reference: chr 9
allele count: 7
allele frequency: 5.80421551881395e-5
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2420C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+31C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+31C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2420C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4592C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4592C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+31C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+31C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+31C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+31C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2420C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8412
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

9-36594801-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594801
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594801
    reference: chr 9
allele count: 1
allele frequency: 8.295863682367972e-6
allele num: 120542
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+33T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2418T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2418T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+33T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+33T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4590T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+33T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2418T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+33T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4590T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+33T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-36594806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594806
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594806
    reference: chr 9
allele count: 8
allele frequency: 6.655020380999917e-5
allele num: 120210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2413C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4585C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+38C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4585C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+38C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+38C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+38C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+38C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2413C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+38C>T
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2413C>T
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

9-36594807-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594807
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594807
    reference: chr 9
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+39G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4584G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+39G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+39G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2412G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+39G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+39G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2412G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+39G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2412G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4584G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

9-36594811-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594811
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594811
    reference: chr 9
allele count: 3
allele frequency: 2.497710432103905e-5
allele num: 120110
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+43T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2408T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+43T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+43T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2408T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4580T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+43T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+43T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4580T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2408T>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+43T>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

9-36594818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594818
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594818
    reference: chr 9
allele count: 1
allele frequency: 8.368901163277262e-6
allele num: 119490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2401G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2401G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+50G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4573G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+50G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+50G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+50G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4573G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2401G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+50G>A
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+50G>A
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

9-36594819-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36594819
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36594819
    reference: chr 9
allele count: 1
allele frequency: 8.368340892734607e-6
allele num: 119498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-2400T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-4572T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.632+51T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.405+51T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.192+51T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-4572T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-301+51T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.405+51T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-2400T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-2400T>G
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.309+51T>G
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

9-36597169-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36597169
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36597169
    reference: chr 9
allele count: 5
allele frequency: 4.253292048045187e-5
allele num: 117556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.193-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-300-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.406-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-2222T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.406-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.310-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.633-50T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-2222T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-50T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15057
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12920
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

9-36597174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36597174
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 36597174
    reference: chr 9
allele count: 745
allele frequency: 6.324385813001918e-3
allele num: 117798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439184
  ensembl transcript: ENST00000536987
  gene symbol: MELK
  hgvsc: ENST00000536987.1:c.13-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000438226
  ensembl transcript: ENST00000538311
  gene symbol: MELK
  hgvsc: ENST00000538311.1:c.-300-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000487398
  gene symbol: MELK
  hgvsc: ENST00000487398.1:n.633-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000443550
  ensembl transcript: ENST00000536329
  gene symbol: MELK
  hgvsc: ENST00000536329.1:c.193-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000441596
  ensembl transcript: ENST00000543751
  gene symbol: MELK
  hgvsc: ENST00000543751.1:c.310-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000437804
  ensembl transcript: ENST00000541717
  gene symbol: MELK
  hgvsc: ENST00000541717.1:c.406-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000489766
  gene symbol: MELK
  hgvsc: ENST00000489766.1:n.411-2217T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000298048
  ensembl transcript: ENST00000298048
  gene symbol: MELK
  hgvsc: ENST00000298048.2:c.406-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000445452
  ensembl transcript: ENST00000545008
  gene symbol: MELK
  hgvsc: ENST00000545008.1:c.262-2217T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl transcript: ENST00000495529
  gene symbol: MELK
  hgvsc: ENST00000495529.1:n.411-45T>C
  variant of: http://identifiers.org/hgnc/16870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165304
  ensembl protein: ENSP00000439792
  ensembl transcript: ENST00000536860
  gene symbol: MELK
  hgvsc: ENST00000536860.1:c.262-45T>C
  variant of: http://identifiers.org/hgnc/16870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18224
  bin: 2.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 1.75e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11169
  bin: 2.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 3.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 1.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 18346
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 3
reference allele: T

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

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

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

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

GenotypeQuality
all individuals: 2395
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13442
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23589
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4044
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4386
bin: 8.25e1
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: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 11576
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: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 6.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

QD
type: SiteQuality
SIO_000300: 1.2e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.559337e6

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

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 13471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5518
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4677
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23589
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4044
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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

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: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.741e1

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.36e-1

DP
type: SiteQuality
SIO_000300: 2.559502e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.072e0

FS
type: SiteQuality
SIO_000300: 5.0e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

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

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

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

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

GenotypeQuality
all individuals: 23589
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2395
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4044
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4677
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5522
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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

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: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.047e0

QD
type: SiteQuality
SIO_000300: 1.322e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.559621e6

MQ
type: SiteQuality
SIO_000300: 5.512e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

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

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

GenotypeQuality
all individuals: 2556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4044
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 23595
bin: 9.75e1
variant carriers: 164

GenotypeQuality
all individuals: 5518
bin: 6.75e1
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: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 134
allele frequency: 1.287718623870844e-2
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: 5
allele frequency: 3.028834504482675e-4
allele num: 16508
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.798507238991637e-4
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.638562543192813e-4
allele num: 11576
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.289e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 2.567175e6

GenotypeQuality
all individuals: 4052
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4687
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4396
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23514
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13519
bin: 6.25e1
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: 908
num of homozygotes: 0

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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
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: 11576
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.408e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.935e0

DP
type: SiteQuality
SIO_000300: 2.55216e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.181e0

GenotypeQuality
all individuals: 13528
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 4
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: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4052
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23513
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4688
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 66736
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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
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QD
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Other
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East Asian
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Latino
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European (Non-Finnish)
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African
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South Asian
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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African
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East Asian
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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East Asian
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South Asian
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Other
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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European (Non-Finnish)
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Other
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African
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South Asian
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Latino
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European (Finnish)
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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East Asian
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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MQ
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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VQSLOD
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FS
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MQ
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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Latino
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South Asian
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European (Finnish)
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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DP
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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Other
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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Latino
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VQSLOD
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DP
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BaseQRankSum
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FS
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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DP
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QD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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African
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VQSLOD
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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BaseQRankSum
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VQSLOD
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MQ
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DP
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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BaseQRankSum
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MQ
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66602
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East Asian
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South Asian
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European (Finnish)
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Other
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Latino
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African
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MQRankSum
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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South Asian
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Latino
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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MQ
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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QD
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MQRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Other
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African
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European (Finnish)
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Latino
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East Asian
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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Latino
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African
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QD
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 4.31e0

InbreedingCoeff
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SIO_000300: 5.7e-3

FS
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MQRankSum
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ClippingRankSum
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SIO_000300: -2.2e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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MQRankSum
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FS
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66624
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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Latino
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Other
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num of homozygotes: 0

DP
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.001860576778802e-5
allele num: 66646
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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Other
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African
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European (Finnish)
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66682
num of homozygotes: 0

South Asian
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Latino
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num of homozygotes: 0

Other
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European (Finnish)
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African
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

African
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European (Non-Finnish)
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num of homozygotes: 0

Other
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European (Finnish)
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East Asian
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South Asian
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QD
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Other
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South Asian
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Latino
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 1.198932949674789e-4
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European (Finnish)
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East Asian
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Other
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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VQSLOD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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allele frequency: 0.0e0
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East Asian
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Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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FS
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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South Asian
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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FS
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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Latino
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Other
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MQ
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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Other
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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Other
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South Asian
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VQSLOD
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FS
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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FS
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ReadPosRankSum
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MQ
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DP
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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SIO_000300: 3.22e0

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.43e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

ReadPosRankSum
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SIO_000300: 1.3e0

FS
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SIO_000300: 4.372e0

ClippingRankSum
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SIO_000300: -1.153e0

QD
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BaseQRankSum
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SIO_000300: 7.7e-2

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 2.417511e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2472
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variant carriers: 0

African
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allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.325e1

FS
type: SiteQuality
SIO_000300: 2.317e0

DP
type: SiteQuality
SIO_000300: 2.41701e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.244e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 6127
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
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: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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

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

FS
type: SiteQuality
SIO_000300: 8.9e0

QD
type: SiteQuality
SIO_000300: 1.201e1

MQRankSum
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SIO_000300: -3.73e-1

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.248e0

DP
type: SiteQuality
SIO_000300: 2.416978e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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: 908
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
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InbreedingCoeff
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QD
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FS
type: SiteQuality
SIO_000300: 4.414e0

MQRankSum
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ClippingRankSum
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SIO_000300: -8.45e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.416728e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
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MQRankSum
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MQ
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FS
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 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: 10400
num of homozygotes: 0

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

South Asian
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allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

Other
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East Asian
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
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: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.993e1

DP
type: SiteQuality
SIO_000300: 2.41392e6

MQ
type: SiteQuality
SIO_000300: 5.845e1

QD
type: SiteQuality
SIO_000300: 9.1e-1

FS
type: SiteQuality
SIO_000300: 7.847e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.715e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 11

GenotypeQuality
all individuals: 14181
bin: 6.25e1
variant carriers: 17

GenotypeQuality
all individuals: 5081
bin: 7.75e1
variant carriers: 14

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 251

GenotypeQuality
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bin: 5.75e1
variant carriers: 17

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 16

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 28

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 15

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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bin: 3.75e1
variant carriers: 18

GenotypeQuality
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variant carriers: 16

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 13

GenotypeQuality
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bin: 9.25e1
variant carriers: 13

Other
type: Population
allele count: 4
allele frequency: 4.524886877828055e-3
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.603262755987504e-4
allele num: 11524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 27
allele frequency: 4.261363636363636e-3
allele num: 6336
num of homozygotes: 0

African
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allele count: 162
allele frequency: 1.639676113360324e-2
allele num: 9880
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 295
allele frequency: 4.507946210268949e-3
allele num: 65440
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 4.6852e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.391e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

QD
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 2.4313e6

VQSLOD
type: SiteQuality
SIO_000300: -1.139e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 5202
bin: 7.75e1
variant carriers: 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: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 8650
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: 16330
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.61e0

QD
type: SiteQuality
SIO_000300: 1.246e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

FS
type: SiteQuality
SIO_000300: 1.7738e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 2.383975e6

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3037
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variant carriers: 0

GenotypeQuality
all individuals: 4324
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: -1.713e0

QD
type: SiteQuality
SIO_000300: 1.831e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

MQ
type: SiteQuality
SIO_000300: 6.037e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.512e0

DP
type: SiteQuality
SIO_000300: 2.383481e6

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
all individuals: 671
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variant carriers: 0

GenotypeQuality
all individuals: 113
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 4975
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 39
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GenotypeQuality
all individuals: 13822
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 4.131e0

QD
type: SiteQuality
SIO_000300: 9.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.342e0

DP
type: SiteQuality
SIO_000300: 2.379065e6

GenotypeQuality
all individuals: 5181
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4976
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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: 8
allele frequency: 1.201670321747229e-4
allele num: 66574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.421150278293135e-4
allele num: 16170
num of homozygotes: 1

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: 11566
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 4.97e-1

BaseQRankSum
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SIO_000300: 4.03e0

DP
type: SiteQuality
SIO_000300: 2.373784e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 1.493e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.883e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

FS
type: SiteQuality
SIO_000300: 8.372999999999999e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

DP
type: SiteQuality
SIO_000300: 2.36495e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.501e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.98e-1

QD
type: SiteQuality
SIO_000300: 1.446e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e0

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

DP
type: SiteQuality
SIO_000300: 2.358654e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19445
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.446e1

DP
type: SiteQuality
SIO_000300: 2.358654e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

FS
type: SiteQuality
SIO_000300: 1.501e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e0

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.98e-1

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 4965
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GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 15984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.772561092938234e-4
allele num: 10394
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-2

FS
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: 8.8e-1

DP
type: SiteQuality
SIO_000300: 2.352059e6

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1004
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19438
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.076e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 2.345379e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.021e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.62e-1

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2928
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 19441
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4959
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1077
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variant carriers: 0

GenotypeQuality
all individuals: 4308
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variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 10380
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.27258844489692e-4
allele num: 15716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.036961171190167e-5
allele num: 66394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.246e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.931e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 2.335722e6

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5120
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15762
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 66442
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.156e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

QD
type: SiteQuality
SIO_000300: 3.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 9.847e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
type: SiteQuality
SIO_000300: 2.33479e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5441
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.889616644191871e-4
allele num: 10382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.326e0

QD
type: SiteQuality
SIO_000300: 1.368e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 2.324054e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 19422
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66256
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 2.310633e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

ClippingRankSum
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SIO_000300: 8.72e-1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.184e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4859
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variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.590220113351786e-5
allele num: 15174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

DP
type: SiteQuality
SIO_000300: 2.310508e6

QD
type: SiteQuality
SIO_000300: 1.003e1

GenotypeQuality
all individuals: 2451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6783
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 13445
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3847
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.943642475776152e-4
allele num: 10114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.48e-1

QD
type: SiteQuality
SIO_000300: 1.631e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

DP
type: SiteQuality
SIO_000300: 1.637215e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 130
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 5.25e1
variant carriers: 5