1-1564698-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564698
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564698
    reference: chr 1
allele count: 2
allele frequency: 4.524886877828054e-5
allele num: 44200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+7C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+7C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2726+7C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

1-1564700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564700
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564700
    reference: chr 1
allele count: 4
allele frequency: 9.097111667045713e-5
allele num: 43970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+9G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+9G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25639
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

1-1564704-A-ACGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564704
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564707
    reference: chr 1
allele count: 855
allele frequency: 1.921261965754348e-2
allele num: 44502
alternate allele: ACGG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+17_2423+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+17_2273+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+17_3686+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+17_512+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+17_2765+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+17_2447+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+17_2423+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+17_*1951+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+17_2726+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+17_1164+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+17_2531+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+17_2714+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+17_2684+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+17_*1159+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+17_206+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+17_2450+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+17_2555+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+17_2001+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+17_2186+19dupCGG
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 1.25e1
  variant carriers: 400
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 12
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

1-1564707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564707
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564707
    reference: chr 1
allele count: 1
allele frequency: 2.293577981651376e-5
allele num: 43600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+16G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+16G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-1564708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564708
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564708
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 43358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+17C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

1-1564710-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564710
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 43168
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+19G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24992
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

1-1564712-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564712
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564712
    reference: chr 1
allele count: 21346
allele frequency: 4.143245341614907e-1
allele num: 51520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+21G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+21G>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 2.5e0
  variant carriers: 847
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 3492
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

1-1564716-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564716
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564716
    reference: chr 1
allele count: 1
allele frequency: 2.848678213309025e-5
allele num: 35104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+25G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+25G>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

1-1564720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564720
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564720
    reference: chr 1
allele count: 1
allele frequency: 3.484320557491289e-5
allele num: 28700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+29C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

1-1564722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564722
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564722
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 28348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2423+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2714+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.512+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2423+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2001+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1164+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1951+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2726+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2447+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2684+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1159+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2450+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2273+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2531+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2555+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3686+31G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2765+31G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

1-1564731-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564731
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564731
    reference: chr 1
allele count: 1
allele frequency: 4.213009774182676e-5
allele num: 23736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+40C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+40C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-34C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-34C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19339
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

1-1564734-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564734
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564733
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 22138
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+47delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+47delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-27delC
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-27delC
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21413
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: GC
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-1564736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564736
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564736
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 20040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+45C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+45C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-29C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-29C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-1564740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564740
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564740
    reference: chr 1
allele count: 2
allele frequency: 1.131349700192329e-4
allele num: 17678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+49C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-25C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+49C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

1-1564742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564742
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564742
    reference: chr 1
allele count: 1
allele frequency: 5.681172594023406e-5
allele num: 17602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+51C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+51C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-23C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-23C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 19078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

1-1564751-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564751
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564751
    reference: chr 1
allele count: 10
allele frequency: 7.26427429899753e-4
allele num: 13766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+60T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+60T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-14T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-14T>G
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

1-1564753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564753
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564753
    reference: chr 1
allele count: 2
allele frequency: 1.548467017652524e-4
allele num: 12916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+62C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+62C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

1-1564758-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564758
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564758
    reference: chr 1
allele count: 1
allele frequency: 9.044862518089724e-5
allele num: 11056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+67C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+67C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-7C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-7C>G
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2727-7C>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

1-1564759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564759
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564759
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 9906
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+68C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+68C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-6C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-6C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2727-6C>T
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP

1-1564761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564761
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564761
    reference: chr 1
allele count: 1
allele frequency: 1.664447403462051e-4
allele num: 6008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+70G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+70G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-4G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-4G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2727-4G>A
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-1564762-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564762
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564762
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 6086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+71C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2766-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1165-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2424-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2685-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.513-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2424-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2002-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2448-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1952-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3687-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1160-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2274-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2715-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+71C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2727-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2532-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2451-3C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2556-3C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2727-3C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS

1-1564768-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564768
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564768
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 5076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2559G>C
  hgvsp: ENSP00000349741.4:p.Glu853Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1168G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+77G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2451G>C
  hgvsp: ENSP00000367982.3:p.Glu817Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2688G>C
  hgvsp: ENSP00000348081.5:p.Glu896Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3690G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2427G>C
  hgvsp: ENSP00000426128.1:p.Glu809Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2005G>C
  hgvsp: ENSP00000427680.1:p.Glu669Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2427G>C
  hgvsp: ENSP00000424615.1:p.Glu809Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2454G>C
  hgvsp: ENSP00000353713.4:p.Glu818Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2718G>C
  hgvsp: ENSP00000428660.1:p.Glu906Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1163G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.516G>C
  hgvsp: ENSP00000464106.1:p.Glu172Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2769G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2535G>C
  hgvsp: ENSP00000428264.1:p.Glu845Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2277G>C
  hgvsp: ENSP00000367980.1:p.Glu759Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2730G>C
  hgvsp: ENSP00000426103.2:p.Glu910Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1955G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+77G>C
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu910Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

1-1564769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564769
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564769
    reference: chr 1
allele count: 2
allele frequency: 3.957261574990107e-4
allele num: 5054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2689C>T
  hgvsp: ENSP00000348081.5:p.Arg897Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1956C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1169C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.517C>T
  hgvsp: ENSP00000464106.1:p.Arg173Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2455C>T
  hgvsp: ENSP00000353713.4:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2006C>T
  hgvsp: ENSP00000427680.1:p.Arg670Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2428C>T
  hgvsp: ENSP00000424615.1:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1164C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+78C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3691C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2731C>T
  hgvsp: ENSP00000426103.2:p.Arg911Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2560C>T
  hgvsp: ENSP00000349741.4:p.Arg854Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2452C>T
  hgvsp: ENSP00000367982.3:p.Arg818Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2770C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+78C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2719C>T
  hgvsp: ENSP00000428660.1:p.Arg907Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2428C>T
  hgvsp: ENSP00000426128.1:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2536C>T
  hgvsp: ENSP00000428264.1:p.Arg846Trp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2278C>T
  hgvsp: ENSP00000367980.1:p.Arg760Trp
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg911Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-1564773-A-AGGCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564773
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564777
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 4728
alternate allele: AGGCG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1967_*1970dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2730_2733dupCGGG
  hgvsp: ENSP00000428660.1:p.Gly912ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2439_2442dupCGGG
  hgvsp: ENSP00000426128.1:p.Gly815ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2700_2703dupCGGG
  hgvsp: ENSP00000348081.5:p.Gly902ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3702_3705dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.528_531dupCGGG
  hgvsp: ENSP00000464106.1:p.Gly178ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2781_2784dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2017_2020dupCGGG
  hgvsp: ENSP00000427680.1:p.Gly675ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+89_2186+92dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2742_2745dupCGGG
  hgvsp: ENSP00000426103.2:p.Gly916ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2439_2442dupCGGG
  hgvsp: ENSP00000424615.1:p.Gly815ArgfsTer34
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+89_206+92dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2463_2466dupCGGG
  hgvsp: ENSP00000367982.3:p.Gly823ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2547_2550dupCGGG
  hgvsp: ENSP00000428264.1:p.Gly851ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1175_*1178dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1180_1183dupCGGG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2466_2469dupCGGG
  hgvsp: ENSP00000353713.4:p.Gly824ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2289_2292dupCGGG
  hgvsp: ENSP00000367980.1:p.Gly765ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2571_2574dupCGGG
  hgvsp: ENSP00000349741.4:p.Gly859ArgfsTer32
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly916ArgfsTer32
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

1-1564774-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564774
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564774
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 2730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3696G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2457G>C
  hgvsp: ENSP00000367982.3:p.Gln819His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1169G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+83G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2775G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2541G>C
  hgvsp: ENSP00000428264.1:p.Gln847His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+83G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2694G>C
  hgvsp: ENSP00000348081.5:p.Gln898His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2736G>C
  hgvsp: ENSP00000426103.2:p.Gln912His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.522G>C
  hgvsp: ENSP00000464106.1:p.Gln174His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1961G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2565G>C
  hgvsp: ENSP00000349741.4:p.Gln855His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2433G>C
  hgvsp: ENSP00000424615.1:p.Gln811His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2433G>C
  hgvsp: ENSP00000426128.1:p.Gln811His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1174G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2724G>C
  hgvsp: ENSP00000428660.1:p.Gln908His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2283G>C
  hgvsp: ENSP00000367980.1:p.Gln761His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2011G>C
  hgvsp: ENSP00000427680.1:p.Gln671His
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2460G>C
  hgvsp: ENSP00000353713.4:p.Gln820His
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln912His
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

1-1564777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564777
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564777
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 3462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1177G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2436G>A
  hgvsp: ENST00000487053.1:c.2436G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2463G>A
  hgvsp: ENST00000360522.4:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2778G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2727G>A
  hgvsp: ENST00000520777.1:c.2727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2568G>A
  hgvsp: ENST00000357210.4:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.525G>A
  hgvsp: ENST00000483015.1:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1172G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2436G>A
  hgvsp: ENST00000504599.1:c.2436G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+86G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2544G>A
  hgvsp: ENST00000518681.1:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1964G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3699G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2739G>A
  hgvsp: ENST00000505820.2:c.2739G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2460G>A
  hgvsp: ENST00000378710.3:c.2460G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2014G>A
  hgvsp: ENST00000514234.1:c.2014G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2286G>A
  hgvsp: ENST00000378708.1:c.2286G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2697G>A
  hgvsp: ENST00000355826.5:c.2697G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+86G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala913Ala
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

1-1564801-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564801
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564801
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 5296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2460C>T
  hgvsp: ENST00000504599.1:c.2460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1196C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2763C>T
  hgvsp: ENST00000505820.2:c.2763C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+110C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1201C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2751C>T
  hgvsp: ENST00000520777.1:c.2751C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2038C>T
  hgvsp: ENST00000514234.1:c.2038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2484C>T
  hgvsp: ENST00000378710.3:c.2484C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3723C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2568C>T
  hgvsp: ENST00000518681.1:c.2568C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2721C>T
  hgvsp: ENST00000355826.5:c.2721C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1988C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+110C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2443+17C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2802C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2487C>T
  hgvsp: ENST00000360522.4:c.2487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2592C>T
  hgvsp: ENST00000357210.4:c.2592C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.549C>T
  hgvsp: ENST00000483015.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2310C>T
  hgvsp: ENST00000378708.1:c.2310C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro921Pro
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

1-1564809-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564809
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564809
    reference: chr 1
allele count: 1
allele frequency: 1.40016802016242e-4
allele num: 7142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2468C>T
  hgvsp: ENSP00000426128.1:p.Thr823Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+118C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2771C>T
  hgvsp: ENSP00000426103.2:p.Thr924Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3731C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2600C>T
  hgvsp: ENSP00000349741.4:p.Thr867Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1209C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+118C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2729C>T
  hgvsp: ENSP00000348081.5:p.Thr910Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2492C>T
  hgvsp: ENSP00000367982.3:p.Thr831Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2759C>T
  hgvsp: ENSP00000428660.1:p.Thr920Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2576C>T
  hgvsp: ENSP00000428264.1:p.Thr859Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2046C>T
  hgvsp: ENSP00000427680.1:p.Thr683Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.557C>T
  hgvsp: ENSP00000464106.1:p.Thr186Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1204C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2495C>T
  hgvsp: ENSP00000353713.4:p.Thr832Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*1996C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2318C>T
  hgvsp: ENSP00000367980.1:p.Thr773Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2810C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2443+25C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr924Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-1564813-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564813
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564813
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 8372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2763C>G
  hgvsp: ENST00000520777.1:c.2763C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1208C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1213C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2050C>G
  hgvsp: ENST00000514234.1:c.2050C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2499C>G
  hgvsp: ENST00000360522.4:c.2499C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.561C>G
  hgvsp: ENST00000483015.1:c.561C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2000C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2496C>G
  hgvsp: ENST00000378710.3:c.2496C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+122C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2580C>G
  hgvsp: ENST00000518681.1:c.2580C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2604C>G
  hgvsp: ENST00000357210.4:c.2604C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2814C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2322C>G
  hgvsp: ENST00000378708.1:c.2322C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2733C>G
  hgvsp: ENST00000355826.5:c.2733C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+122C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2472C>G
  hgvsp: ENST00000504599.1:c.2472C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2443+29C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3735C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2775C>G
  hgvsp: ENST00000505820.2:c.2775C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu925Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-1564818-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564818
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564818
    reference: chr 1
allele count: 1
allele frequency: 1.05241001894338e-4
allele num: 9502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2501C>A
  hgvsp: ENSP00000367982.3:p.Thr834Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2055C>A
  hgvsp: ENSP00000427680.1:p.Thr686Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2609C>A
  hgvsp: ENSP00000349741.4:p.Thr870Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2327C>A
  hgvsp: ENSP00000367980.1:p.Thr776Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2819C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1218C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2780C>A
  hgvsp: ENSP00000426103.2:p.Thr927Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1213C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2504C>A
  hgvsp: ENSP00000353713.4:p.Thr835Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+127C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2585C>A
  hgvsp: ENSP00000428264.1:p.Thr862Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2005C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2768C>A
  hgvsp: ENSP00000428660.1:p.Thr923Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2477C>A
  hgvsp: ENSP00000426128.1:p.Thr826Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+127C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2738C>A
  hgvsp: ENSP00000348081.5:p.Thr913Asn
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2443+34C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3740C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.566C>A
  hgvsp: ENSP00000464106.1:p.Thr189Asn
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr927Asn
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

1-1564822-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564822
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564822
    reference: chr 1
allele count: 2
allele frequency: 2.002002002002002e-4
allele num: 9990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1222C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1217C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2742C>G
  hgvsp: ENST00000355826.5:c.2742C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+131C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2772C>G
  hgvsp: ENST00000520777.1:c.2772C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2613C>G
  hgvsp: ENST00000357210.4:c.2613C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3744C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2784C>G
  hgvsp: ENST00000505820.2:c.2784C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2059C>G
  hgvsp: ENST00000514234.1:c.2059C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2508C>G
  hgvsp: ENST00000360522.4:c.2508C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2481C>G
  hgvsp: ENST00000504599.1:c.2481C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2589C>G
  hgvsp: ENST00000518681.1:c.2589C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2009C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2505C>G
  hgvsp: ENST00000378710.3:c.2505C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2443+38C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2823C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.570C>G
  hgvsp: ENST00000483015.1:c.570C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+131C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2331C>G
  hgvsp: ENST00000378708.1:c.2331C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro928Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

1-1564825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564825
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564825
    reference: chr 1
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1225C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2592C>T
  hgvsp: ENST00000518681.1:c.2592C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2787C>T
  hgvsp: ENST00000505820.2:c.2787C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2062C>T
  hgvsp: ENST00000514234.1:c.2062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1220C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2508C>T
  hgvsp: ENST00000378710.3:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2745C>T
  hgvsp: ENST00000355826.5:c.2745C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2484C>T
  hgvsp: ENST00000504599.1:c.2484C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3747C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2511C>T
  hgvsp: ENST00000360522.4:c.2511C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2334C>T
  hgvsp: ENST00000378708.1:c.2334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2826C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2616C>T
  hgvsp: ENST00000357210.4:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2775C>T
  hgvsp: ENST00000520777.1:c.2775C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2012C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2443+41C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.573C>T
  hgvsp: ENST00000483015.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+134C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+134C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn929Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-1564837-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564837
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564837
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 10640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2787C>G
  hgvsp: ENSP00000428660.1:p.Asn929Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2604C>G
  hgvsp: ENSP00000428264.1:p.Asn868Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2346C>G
  hgvsp: ENSP00000367980.1:p.Asn782Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.585C>G
  hgvsp: ENSP00000464106.1:p.Asn195Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1232C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2523C>G
  hgvsp: ENSP00000353713.4:p.Asn841Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3759C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+146C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2024C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2074C>G
  hgvsp: ENSP00000427680.1:p.Asn692Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2496C>G
  hgvsp: ENSP00000426128.1:p.Asn832Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1237C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2520C>G
  hgvsp: ENSP00000367982.3:p.Asn840Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2838C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2628C>G
  hgvsp: ENSP00000349741.4:p.Asn876Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2799C>G
  hgvsp: ENSP00000426103.2:p.Asn933Lys
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-31C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+146C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2757C>G
  hgvsp: ENSP00000348081.5:p.Asn919Lys
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn933Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

1-1564838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564838
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564838
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 10654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3760C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2524C>T
  hgvsp: ENST00000360522.4:c.2524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2629C>T
  hgvsp: ENST00000357210.4:c.2629C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2521C>T
  hgvsp: ENST00000378710.3:c.2521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2788C>T
  hgvsp: ENST00000520777.1:c.2788C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2347C>T
  hgvsp: ENST00000378708.1:c.2347C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2839C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2800C>T
  hgvsp: ENST00000505820.2:c.2800C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2025C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2497C>T
  hgvsp: ENST00000504599.1:c.2497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1233C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+147C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2605C>T
  hgvsp: ENST00000518681.1:c.2605C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2075C>T
  hgvsp: ENST00000514234.1:c.2075C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2758C>T
  hgvsp: ENST00000355826.5:c.2758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.586C>T
  hgvsp: ENST00000483015.1:c.586C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1238C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+147C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-30C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu934Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-1564846-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564846
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564846
    reference: chr 1
allele count: 1
allele frequency: 9.240436148586214e-5
allele num: 10822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2613G>C
  hgvsp: ENST00000518681.1:c.2613G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2796G>C
  hgvsp: ENST00000520777.1:c.2796G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2529G>C
  hgvsp: ENST00000378710.3:c.2529G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2766G>C
  hgvsp: ENST00000355826.5:c.2766G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2355G>C
  hgvsp: ENST00000378708.1:c.2355G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2532G>C
  hgvsp: ENST00000360522.4:c.2532G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2808G>C
  hgvsp: ENST00000505820.2:c.2808G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2505G>C
  hgvsp: ENST00000504599.1:c.2505G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.594G>C
  hgvsp: ENST00000483015.1:c.594G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2637G>C
  hgvsp: ENST00000357210.4:c.2637G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2847G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2083G>C
  hgvsp: ENST00000514234.1:c.2083G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2033G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3768G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1241G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+155G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+155G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1246G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-22G>C
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val936Val
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

1-1564849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564849
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564849
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 10864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2799C>T
  hgvsp: ENST00000520777.1:c.2799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2850C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2532C>T
  hgvsp: ENST00000378710.3:c.2532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2086C>T
  hgvsp: ENST00000514234.1:c.2086C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.597C>T
  hgvsp: ENST00000483015.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2036C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2769C>T
  hgvsp: ENST00000355826.5:c.2769C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2640C>T
  hgvsp: ENST00000357210.4:c.2640C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2616C>T
  hgvsp: ENST00000518681.1:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2358C>T
  hgvsp: ENST00000378708.1:c.2358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1244C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-19C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2508C>T
  hgvsp: ENST00000504599.1:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1249C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2811C>T
  hgvsp: ENST00000505820.2:c.2811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3771C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2535C>T
  hgvsp: ENST00000360522.4:c.2535C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2186+158C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.206+158C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly937Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

1-1564857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564857
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564857
    reference: chr 1
allele count: 1
allele frequency: 9.054690329590728e-5
allele num: 11044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2094C>T
  hgvsp: ENSP00000427680.1:p.Pro699Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2540C>T
  hgvsp: ENSP00000367982.3:p.Pro847Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2648C>T
  hgvsp: ENSP00000349741.4:p.Pro883Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.605C>T
  hgvsp: ENSP00000464106.1:p.Pro202Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2516C>T
  hgvsp: ENSP00000426128.1:p.Pro839Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1252C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2624C>T
  hgvsp: ENSP00000428264.1:p.Pro875Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3779C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-11C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2777C>T
  hgvsp: ENSP00000348081.5:p.Pro926Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2819C>T
  hgvsp: ENSP00000426103.2:p.Pro940Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1257C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2543C>T
  hgvsp: ENSP00000353713.4:p.Pro848Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2807C>T
  hgvsp: ENSP00000428660.1:p.Pro936Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2366C>T
  hgvsp: ENSP00000367980.1:p.Pro789Leu
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-162C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.5C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2044C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2858C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-162C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro940Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

1-1564858-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564858
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564858
    reference: chr 1
allele count: 18
allele frequency: 1.618996222342148e-3
allele num: 11118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2095G>A
  hgvsp: ENST00000514234.1:c.2095G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2367G>A
  hgvsp: ENST00000378708.1:c.2367G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2778G>A
  hgvsp: ENST00000355826.5:c.2778G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2625G>A
  hgvsp: ENST00000518681.1:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-10G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2649G>A
  hgvsp: ENST00000357210.4:c.2649G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.606G>A
  hgvsp: ENST00000483015.1:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3780G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2544G>A
  hgvsp: ENST00000360522.4:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2808G>A
  hgvsp: ENST00000520777.1:c.2808G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-161G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-161G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.6G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2820G>A
  hgvsp: ENST00000505820.2:c.2820G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2045G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2517G>A
  hgvsp: ENST00000504599.1:c.2517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2859G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2541G>A
  hgvsp: ENST00000378710.3:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1253G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1258G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro940Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-1564864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564864
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564864
    reference: chr 1
allele count: 3
allele frequency: 2.660517914153955e-4
allele num: 11276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1264C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2051C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-155C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.612C>T
  hgvsp: ENST00000483015.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2784C>T
  hgvsp: ENST00000355826.5:c.2784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.12C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2373C>T
  hgvsp: ENST00000378708.1:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2814C>T
  hgvsp: ENST00000520777.1:c.2814C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2631C>T
  hgvsp: ENST00000518681.1:c.2631C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2655C>T
  hgvsp: ENST00000357210.4:c.2655C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2547C>T
  hgvsp: ENST00000378710.3:c.2547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2101C>T
  hgvsp: ENST00000514234.1:c.2101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-155C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2550C>T
  hgvsp: ENST00000360522.4:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2826C>T
  hgvsp: ENST00000505820.2:c.2826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.2444-4C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1259C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3786C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2523C>T
  hgvsp: ENST00000504599.1:c.2523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2444-4C>T
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

1-1564880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564880
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564880
    reference: chr 1
allele count: 1
allele frequency: 8.465966813410092e-5
allele num: 11812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1280C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.28C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.628C>T
  hgvsp: ENST00000483015.1:c.628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2563C>T
  hgvsp: ENST00000378710.3:c.2563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2842C>T
  hgvsp: ENST00000505820.2:c.2842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2539C>T
  hgvsp: ENST00000504599.1:c.2539C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2800C>T
  hgvsp: ENST00000355826.5:c.2800C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2671C>T
  hgvsp: ENST00000357210.4:c.2671C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3802C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2389C>T
  hgvsp: ENST00000378708.1:c.2389C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2067C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2881C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-139C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2647C>T
  hgvsp: ENST00000518681.1:c.2647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-139C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2566C>T
  hgvsp: ENST00000360522.4:c.2566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2830C>T
  hgvsp: ENST00000520777.1:c.2830C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2117C>T
  hgvsp: ENST00000514234.1:c.2117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1275C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu948Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

1-1564894-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564894
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564894
    reference: chr 1
allele count: 2
allele frequency: 1.633186346562143e-4
allele num: 12246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2580G>A
  hgvsp: ENST00000360522.4:c.2580G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1294G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2131G>A
  hgvsp: ENST00000514234.1:c.2131G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2814G>A
  hgvsp: ENST00000355826.5:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2856G>A
  hgvsp: ENST00000505820.2:c.2856G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2685G>A
  hgvsp: ENST00000357210.4:c.2685G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.642G>A
  hgvsp: ENST00000483015.1:c.642G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2403G>A
  hgvsp: ENST00000378708.1:c.2403G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2577G>A
  hgvsp: ENST00000378710.3:c.2577G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2661G>A
  hgvsp: ENST00000518681.1:c.2661G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2844G>A
  hgvsp: ENST00000520777.1:c.2844G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3816G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2553G>A
  hgvsp: ENST00000504599.1:c.2553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-125G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2895G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1289G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.42G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-125G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2081G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu952Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

1-1564894-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564894
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564894
    reference: chr 1
allele count: 1
allele frequency: 8.165931732810714e-5
allele num: 12246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1289G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2131G>C
  hgvsp: ENSP00000427680.1:p.Glu711Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2403G>C
  hgvsp: ENSP00000367980.1:p.Glu801Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3816G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2856G>C
  hgvsp: ENSP00000426103.2:p.Glu952Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2580G>C
  hgvsp: ENSP00000353713.4:p.Glu860Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-125G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-125G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2844G>C
  hgvsp: ENSP00000428660.1:p.Glu948Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2553G>C
  hgvsp: ENSP00000426128.1:p.Glu851Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2577G>C
  hgvsp: ENSP00000367982.3:p.Glu859Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2814G>C
  hgvsp: ENSP00000348081.5:p.Glu938Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2081G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2661G>C
  hgvsp: ENSP00000428264.1:p.Glu887Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.642G>C
  hgvsp: ENSP00000464106.1:p.Glu214Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2685G>C
  hgvsp: ENSP00000349741.4:p.Glu895Asp
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.42G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2895G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1294G>C
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu952Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/1-1564895-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564895
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564895
    reference: chr 1
allele count: 6
allele frequency: 4.888381945576015e-4
allele num: 12274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2554C>A
  hgvsp: ENSP00000426128.1:p.Leu852Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-124C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2845C>A
  hgvsp: ENSP00000428660.1:p.Leu949Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2815C>A
  hgvsp: ENSP00000348081.5:p.Leu939Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*20C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2857C>A
  hgvsp: ENSP00000426103.2:p.Leu953Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2082C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2686C>A
  hgvsp: ENSP00000349741.4:p.Leu896Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1295C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.43C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2896C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2404C>A
  hgvsp: ENSP00000367980.1:p.Leu802Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2578C>A
  hgvsp: ENSP00000367982.3:p.Leu860Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2132C>A
  hgvsp: ENSP00000427680.1:p.Leu712Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2662C>A
  hgvsp: ENSP00000428264.1:p.Leu888Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1290C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.643C>A
  hgvsp: ENSP00000464106.1:p.Leu215Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3817C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2581C>A
  hgvsp: ENSP00000353713.4:p.Leu861Met
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-124C>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu953Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

1-1564901-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564901
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564901
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 12564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.49C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2138C>G
  hgvsp: ENSP00000427680.1:p.Leu714Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2584C>G
  hgvsp: ENSP00000367982.3:p.Leu862Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1301C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2088C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3823C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1296C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2821C>G
  hgvsp: ENSP00000348081.5:p.Leu941Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2902C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.649C>G
  hgvsp: ENSP00000464106.1:p.Leu217Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2560C>G
  hgvsp: ENSP00000426128.1:p.Leu854Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2410C>G
  hgvsp: ENSP00000367980.1:p.Leu804Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2668C>G
  hgvsp: ENSP00000428264.1:p.Leu890Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-118C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2863C>G
  hgvsp: ENSP00000426103.2:p.Leu955Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2692C>G
  hgvsp: ENSP00000349741.4:p.Leu898Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2587C>G
  hgvsp: ENSP00000353713.4:p.Leu863Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2851C>G
  hgvsp: ENSP00000428660.1:p.Leu951Val
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-118C>G
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu955Val
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

1-1564903-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564903
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564903
    reference: chr 1
allele count: 1
allele frequency: 7.854225573358467e-5
allele num: 12732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2670G>C
  hgvsp: ENST00000518681.1:c.2670G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2853G>C
  hgvsp: ENST00000520777.1:c.2853G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.651G>C
  hgvsp: ENST00000483015.1:c.651G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2090G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2562G>C
  hgvsp: ENST00000504599.1:c.2562G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2904G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*28G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1298G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2140G>C
  hgvsp: ENST00000514234.1:c.2140G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2589G>C
  hgvsp: ENST00000360522.4:c.2589G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3825G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2865G>C
  hgvsp: ENST00000505820.2:c.2865G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2412G>C
  hgvsp: ENST00000378708.1:c.2412G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2823G>C
  hgvsp: ENST00000355826.5:c.2823G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2694G>C
  hgvsp: ENST00000357210.4:c.2694G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2586G>C
  hgvsp: ENST00000378710.3:c.2586G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-116G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-116G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1303G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.51G>C
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu955Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

1-1564909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564909
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564909
    reference: chr 1
allele count: 1
allele frequency: 7.568876778686043e-5
allele num: 13212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2595G>A
  hgvsp: ENST00000360522.4:c.2595G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2568G>A
  hgvsp: ENST00000504599.1:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2096G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2676G>A
  hgvsp: ENST00000518681.1:c.2676G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2871G>A
  hgvsp: ENST00000505820.2:c.2871G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2700G>A
  hgvsp: ENST00000357210.4:c.2700G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-110G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2592G>A
  hgvsp: ENST00000378710.3:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2146G>A
  hgvsp: ENST00000514234.1:c.2146G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.657G>A
  hgvsp: ENST00000483015.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000473511
  gene symbol: MIB2
  hgvsc: ENST00000473511.1:n.1309G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2859G>A
  hgvsp: ENST00000520777.1:c.2859G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.57G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2829G>A
  hgvsp: ENST00000355826.5:c.2829G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2418G>A
  hgvsp: ENST00000378708.1:c.2418G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1304G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3831G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2910G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-110G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val957Val
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

1-1564939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564939
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564939
    reference: chr 1
allele count: 4
allele frequency: 2.23563603845294e-4
allele num: 17892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2176G>A
  hgvsp: ENST00000514234.1:c.2176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2940G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2901G>A
  hgvsp: ENST00000505820.2:c.2901G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2625G>A
  hgvsp: ENST00000360522.4:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2706G>A
  hgvsp: ENST00000518681.1:c.2706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2889G>A
  hgvsp: ENST00000520777.1:c.2889G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2126G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*64G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2622G>A
  hgvsp: ENST00000378710.3:c.2622G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.87G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2598G>A
  hgvsp: ENST00000504599.1:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2859G>A
  hgvsp: ENST00000355826.5:c.2859G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2448G>A
  hgvsp: ENST00000378708.1:c.2448G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-80G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.687G>A
  hgvsp: ENST00000483015.1:c.687G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2730G>A
  hgvsp: ENST00000357210.4:c.2730G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1334G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3861G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-80G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val967Val
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

1-1564949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564949
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564949
    reference: chr 1
allele count: 3
allele frequency: 1.601537475976938e-4
allele num: 18732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-70G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.97G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-70G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+3G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+3G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2908+3G>A
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-1564952-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564952
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564953
    reference: chr 1
allele count: 43
allele frequency: 1.199040767386091e-3
allele num: 35862
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.106dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-61dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+12dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-61dupG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+12dupG
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2908+12dupG
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

1-1564952-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564952
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564951
    reference: chr 1
allele count: 14413
allele frequency: 4.019017344264124e-1
allele num: 35862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-61delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-61delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+12delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.106delG
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+12delG
  variant of: http://identifiers.org/hgnc/30577
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2908+12delG
num of homozygotes: 2435
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: TG
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

1-1564958-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564958
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564958
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 38128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-61G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.106G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-61G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+12G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+12G>C
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

1-1564958-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564958
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564958
    reference: chr 1
allele count: 1
allele frequency: 2.622744439781788e-5
allele num: 38128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.106G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-61G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+12G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-61G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-1564959-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564959
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564959
    reference: chr 1
allele count: 1
allele frequency: 2.628397203385376e-5
allele num: 38046
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-60C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.107C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-60C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+13C>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+13C>A
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

1-1564959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564959
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564959
    reference: chr 1
allele count: 2
allele frequency: 5.256794406770751e-5
allele num: 38046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-60C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.107C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+13C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-60C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+13C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10698
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

1-1564964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564964
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564964
    reference: chr 1
allele count: 1
allele frequency: 2.473288484368817e-5
allele num: 40432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-55G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.112G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+18G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-55G>A
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+18G>A
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

1-1564965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564965
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564965
    reference: chr 1
allele count: 1
allele frequency: 2.450620006861736e-5
allele num: 40806
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-54G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.113G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-54G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+19G>C
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+19G>C
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

1-1564967-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564967
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564967
    reference: chr 1
allele count: 1
allele frequency: 2.455192732629511e-5
allele num: 40730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.115T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-52T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-52T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+21T>G
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+21T>G
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-1564969-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564969
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564969
    reference: chr 1
allele count: 3
allele frequency: 7.098911500236631e-5
allele num: 42260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-50G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-50G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.117G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+23G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+23G>T
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-1564974-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564974
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564974
    reference: chr 1
allele count: 1
allele frequency: 2.265724125430488e-5
allele num: 44136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-45G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.122G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-45G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+28G>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+28G>T
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30002
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

1-1564976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564976
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564976
    reference: chr 1
allele count: 1
allele frequency: 2.21690165824244e-5
allele num: 45108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.124C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-43C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-43C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+30C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+30C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

1-1564977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1564977
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 1564977
    reference: chr 1
allele count: 3
allele frequency: 6.605019815059445e-5
allele num: 45420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000425032
  ensembl transcript: ENST00000506488
  gene symbol: MIB2
  hgvsc: ENST00000506488.1:c.*1341+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511502
  gene symbol: MIB2
  hgvsc: ENST00000511502.1:n.2947+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000470373
  gene symbol: MIB2
  hgvsc: ENST00000470373.1:n.125C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367980
  ensembl transcript: ENST00000378708
  gene symbol: MIB2
  hgvsc: ENST00000378708.1:c.2455+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367982
  ensembl transcript: ENST00000378710
  gene symbol: MIB2
  hgvsc: ENST00000378710.3:c.2629+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000427680
  ensembl transcript: ENST00000514234
  gene symbol: MIB2
  hgvsc: ENST00000514234.1:c.2183+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000511910
  gene symbol: MIB2
  hgvsc: ENST00000511910.1:n.207-42C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426007
  ensembl transcript: ENST00000489635
  gene symbol: MIB2
  hgvsc: ENST00000489635.1:c.*2133+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000348081
  ensembl transcript: ENST00000355826
  gene symbol: MIB2
  hgvsc: ENST00000355826.5:c.2866+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428264
  ensembl transcript: ENST00000518681
  gene symbol: MIB2
  hgvsc: ENST00000518681.1:c.2713+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000424615
  ensembl transcript: ENST00000487053
  gene symbol: MIB2
  hgvsc: ENST00000487053.1:c.*71+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000353713
  ensembl transcript: ENST00000360522
  gene symbol: MIB2
  hgvsc: ENST00000360522.4:c.2632+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426128
  ensembl transcript: ENST00000504599
  gene symbol: MIB2
  hgvsc: ENST00000504599.1:c.2605+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000464106
  ensembl transcript: ENST00000483015
  gene symbol: MIB2
  hgvsc: ENST00000483015.1:c.694+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000426103
  ensembl transcript: ENST00000505820
  gene symbol: MIB2
  hgvsc: ENST00000505820.2:c.2908+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl transcript: ENST00000479659
  gene symbol: MIB2
  hgvsc: ENST00000479659.1:n.3868+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000428660
  ensembl transcript: ENST00000520777
  gene symbol: MIB2
  hgvsc: ENST00000520777.1:c.2896+31C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000367984
  ensembl transcript: ENST00000378712
  gene symbol: MIB2
  hgvsc: ENST00000378712.1:c.2187-42C>T
  variant of: http://identifiers.org/hgnc/30577
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197530
  ensembl protein: ENSP00000349741
  ensembl transcript: ENST00000357210
  gene symbol: MIB2
  hgvsc: ENST00000357210.4:c.2737+31C>T
  variant of: http://identifiers.org/hgnc/30577
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C

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

GenotypeDepth
all individuals: 9177
bin: 1.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1523
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7939
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7646
bin: 2.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 161
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 25871
bin: 7.5e0
variant carriers: 0

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

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

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

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

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

GenotypeDepth
all individuals: 4170
bin: 1.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 679
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8699
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27150
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 613
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.819709702062643e-4
allele num: 5236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25772
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.876e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-1

QD
type: SiteQuality
SIO_000300: 2.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

DP
type: SiteQuality
SIO_000300: 6.02899e5

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

FS
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
all individuals: 1572
bin: 2.75e1
variant carriers: 1

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

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

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

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

GenotypeDepth
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7998
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 9313
bin: 1.25e1
variant carriers: 0

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

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

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

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

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

GenotypeDepth
all individuals: 175
bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2440
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8818
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 714
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1563
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26768
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.915426781519186e-4
allele num: 5108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.77363184079602e-5
allele num: 25728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2532
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5104
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

VQSLOD
type: SiteQuality
SIO_000300: -2.845e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 6.582e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

DP
type: SiteQuality
SIO_000300: 6.01318e5

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

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

GenotypeDepth
all individuals: 1517
bin: 2.75e1
variant carriers: 37

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

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

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

GenotypeDepth
all individuals: 7170
bin: 2.25e1
variant carriers: 121

GenotypeDepth
all individuals: 3
bin: 4.25e1
variant carriers: 3

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

GenotypeDepth
all individuals: 25504
bin: 7.5e0
variant carriers: 277

GenotypeDepth
all individuals: 164
bin: 3.25e1
variant carriers: 16

GenotypeDepth
all individuals: 8079
bin: 2.5e0
variant carriers: 26

GenotypeDepth
all individuals: 13
bin: 3.75e1
variant carriers: 6

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

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

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

GenotypeDepth
all individuals: 4264
bin: 1.75e1
variant carriers: 260

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1132
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 18

GenotypeQuality
all individuals: 1551
bin: 1.25e1
variant carriers: 8

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 79
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 994
bin: 9.75e1
variant carriers: 994

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 31

GenotypeQuality
all individuals: 2211
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 775
bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 6410
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 25853
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 8684
bin: 7.5e0
variant carriers: 6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 493
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variant carriers: 6

GenotypeQuality
all individuals: 1774
bin: 3.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2034
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 116
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variant carriers: 7

GenotypeQuality
all individuals: 2384
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 613
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 21
allele frequency: 4.174950298210736e-3
allele num: 5030
num of homozygotes: 0

Latino
type: Population
allele count: 96
allele frequency: 1.840490797546012e-2
allele num: 5216
num of homozygotes: 2

African
type: Population
allele count: 13
allele frequency: 5.195843325339729e-3
allele num: 2502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 716
allele frequency: 2.727411244857535e-2
allele num: 26252
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.367989056087551e-3
allele num: 1462
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 2.573529411764706e-2
allele num: 272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3768
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 1.595e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.766e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 5.95437e5

GenotypeDepth
all individuals: 25361
bin: 7.5e0
variant carriers: 1

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

GenotypeDepth
all individuals: 1486
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8436
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 6716
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 173
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 25647
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variant carriers: 0

GenotypeQuality
all individuals: 1766
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 4.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2528
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variant carriers: 0

GenotypeQuality
all individuals: 2319
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 861
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variant carriers: 0

GenotypeQuality
all individuals: 9148
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GenotypeQuality
all individuals: 826
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variant carriers: 0

GenotypeQuality
all individuals: 5537
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variant carriers: 0

GenotypeQuality
all individuals: 2681
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 279
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1452
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.079866888519135e-4
allele num: 4808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.85044e5

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.616e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 9671
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 179
bin: 3.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 8447
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variant carriers: 0

GenotypeDepth
all individuals: 1523
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 6674
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variant carriers: 0

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

GenotypeDepth
all individuals: 4213
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 25273
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 0
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variant carriers: 0

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

GenotypeDepth
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

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

GenotypeQuality
all individuals: 672
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
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variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5612
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variant carriers: 0

GenotypeQuality
all individuals: 9198
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2559
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25656
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5078
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4744
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

QD
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.93e0

DP
type: SiteQuality
SIO_000300: 5.85948e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

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

GenotypeDepth
all individuals: 187
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 8637
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 1573
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6208
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 4193
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

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

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 9399
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1027
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4808
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.363e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

DP
type: SiteQuality
SIO_000300: 5.79669e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.179e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

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

GenotypeDepth
all individuals: 1915
bin: 2.75e1
variant carriers: 1230

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

GenotypeDepth
all individuals: 19488
bin: 7.5e0
variant carriers: 5859

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

GenotypeDepth
all individuals: 6753
bin: 1.75e1
variant carriers: 5784

GenotypeDepth
all individuals: 116
bin: 3.75e1
variant carriers: 113

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

GenotypeDepth
all individuals: 27
bin: 4.75e1
variant carriers: 27

GenotypeDepth
all individuals: 13311
bin: 1.25e1
variant carriers: 7708

GenotypeDepth
all individuals: 4660
bin: 2.25e1
variant carriers: 2904

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 5

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 1

GenotypeDepth
all individuals: 69
bin: 4.25e1
variant carriers: 68

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 10

GenotypeDepth
all individuals: 546
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variant carriers: 466

GenotypeQuality
all individuals: 604
bin: 8.75e1
variant carriers: 604

GenotypeQuality
all individuals: 625
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variant carriers: 625

GenotypeQuality
all individuals: 6938
bin: 7.5e0
variant carriers: 580

GenotypeQuality
all individuals: 777
bin: 5.25e1
variant carriers: 714

GenotypeQuality
all individuals: 614
bin: 4.25e1
variant carriers: 520

GenotypeQuality
all individuals: 3917
bin: 2.5e0
variant carriers: 151

GenotypeQuality
all individuals: 12464
bin: 9.75e1
variant carriers: 12464

GenotypeQuality
all individuals: 803
bin: 6.75e1
variant carriers: 654

GenotypeQuality
all individuals: 1195
bin: 1.25e1
variant carriers: 619

GenotypeQuality
all individuals: 689
bin: 4.75e1
variant carriers: 612

GenotypeQuality
all individuals: 1681
bin: 1.75e1
variant carriers: 959

GenotypeQuality
all individuals: 1381
bin: 3.25e1
variant carriers: 817

GenotypeQuality
all individuals: 15213
bin: 2.25e1
variant carriers: 1037

GenotypeQuality
all individuals: 1613
bin: 2.75e1
variant carriers: 802

GenotypeQuality
all individuals: 585
bin: 7.25e1
variant carriers: 578

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 626

GenotypeQuality
all individuals: 787
bin: 5.75e1
variant carriers: 666

GenotypeQuality
all individuals: 2624
bin: 6.25e1
variant carriers: 707

GenotypeQuality
all individuals: 605
bin: 7.75e1
variant carriers: 598

GenotypeQuality
all individuals: 977
bin: 3.75e1
variant carriers: 705

South Asian
type: Population
allele count: 2002
allele frequency: 3.711531331108639e-1
allele num: 5394
num of homozygotes: 304

European (Finnish)
type: Population
allele count: 1040
allele frequency: 5.123152709359606e-1
allele num: 2030
num of homozygotes: 199

East Asian
type: Population
allele count: 1373
allele frequency: 3.334142787761049e-1
allele num: 4118
num of homozygotes: 162

European (Non-Finnish)
type: Population
allele count: 14138
allele frequency: 4.54189154459008e-1
allele num: 31128
num of homozygotes: 2510

Latino
type: Population
allele count: 2371
allele frequency: 3.872917347272133e-1
allele num: 6122
num of homozygotes: 288

African
type: Population
allele count: 300
allele frequency: 1.246882793017456e-1
allele num: 2406
num of homozygotes: 13

Other
type: Population
allele count: 122
allele frequency: 3.788819875776397e-1
allele num: 322
num of homozygotes: 16

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 6.1783e5

FS
type: SiteQuality
SIO_000300: 1.938e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.240000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.72e0

QD
type: SiteQuality
SIO_000300: 1.482e1

GenotypeDepth
all individuals: 12930
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1357
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variant carriers: 0

GenotypeDepth
all individuals: 22763
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 1874
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 236
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 14504
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GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 2
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variant carriers: 1

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 627
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variant carriers: 1

GenotypeQuality
all individuals: 1992
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variant carriers: 0

GenotypeQuality
all individuals: 28953
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GenotypeQuality
all individuals: 1363
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 2.5e0
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GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1226
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European (Non-Finnish)
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South Asian
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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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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FS
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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African
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Latino
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East 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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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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QD
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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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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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MQ
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DP
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FS
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Latino
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African
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European (Finnish)
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South Asian
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FS
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QD
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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African
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Other
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European (Non-Finnish)
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allele num: 10420
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South Asian
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BaseQRankSum
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FS
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MQ
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DP
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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MQ
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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allele num: 2030
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Latino
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European (Non-Finnish)
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allele num: 7928
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Other
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African
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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allele num: 7420
num of homozygotes: 0

African
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num of homozygotes: 0

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

East Asian
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Other
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

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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European (Non-Finnish)
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allele num: 6202
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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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FS
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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East Asian
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QD
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MQRankSum
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FS
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African
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East Asian
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FS
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MQ
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VQSLOD
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BaseQRankSum
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DP
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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MQ
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DP
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European (Finnish)
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African
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East Asian
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South Asian
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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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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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DP
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ReadPosRankSum
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MQ
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FS
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQRankSum
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FS
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Other
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FS
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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African
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East Asian
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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QD
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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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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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East Asian
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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DP
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QD
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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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African
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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DP
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FS
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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GenotypeDepth
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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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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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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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ClippingRankSum
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DP
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MQRankSum
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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African
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European (Non-Finnish)
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South Asian
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Latino
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Other
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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Other
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South Asian
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African
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European (Finnish)
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East Asian
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FS
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BaseQRankSum
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QD
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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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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European (Non-Finnish)
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FS
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ClippingRankSum
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VQSLOD
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QD
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20852
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.664e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.73e-2

DP
type: SiteQuality
SIO_000300: 1.84556e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeDepth
all individuals: 25466
bin: 2.5e0
variant carriers: 1

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

GenotypeDepth
all individuals: 4061
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 135
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1893
bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 324
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1361
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21904
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3574
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2788
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.246376811594203e-3
allele num: 138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.016e-1

DP
type: SiteQuality
SIO_000300: 1.89974e5

QD
type: SiteQuality
SIO_000300: 1.468e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.790000000000001e-2

FS
type: SiteQuality
SIO_000300: 7.611e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

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

GenotypeDepth
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 0
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variant carriers: 0

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

GenotypeDepth
all individuals: 1946
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 137
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 25919
bin: 2.5e0
variant carriers: 1

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

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

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4064
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 170
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3859
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 447
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22084
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4649
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.88e0

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.91e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.91477e5

VQSLOD
type: SiteQuality
SIO_000300: -2.273e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeDepth
all individuals: 1063
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 177
bin: 3.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 29126
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2370
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 1.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 50
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4084
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 1
bin: 4.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3405
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25748
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 261
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4683
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.346257404415724e-4
allele num: 7428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.87e-2

DP
type: SiteQuality
SIO_000300: 2.03584e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.969999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.01e-1

QD
type: SiteQuality
SIO_000300: 1.092e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

GenotypeDepth
all individuals: 29451
bin: 2.5e0
variant carriers: 24

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

GenotypeDepth
all individuals: 4086
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1067
bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 188
bin: 1.25e1
variant carriers: 10

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

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

GenotypeDepth
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 179
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2464
bin: 7.5e0
variant carriers: 36

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

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

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 51
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 9
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 450
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1787
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 25875
bin: 7.5e0
variant carriers: 12

GenotypeQuality
all individuals: 4687
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3576
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 405
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.25e1
variant carriers: 4

African
type: Population
allele count: 18
allele frequency: 5.0e-2
allele num: 360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.456e1

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

DP
type: SiteQuality
SIO_000300: 2.05697e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000197530
ensembl transcript: ENST00000511502
gene symbol: MIB2
hgvsc: ENST00000511502.1:n.2865C>T
variant of: http://identifiers.org/hgnc/30577

GenotypeDepth
all individuals: 221
bin: 1.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 2

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

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

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

GenotypeDepth
all individuals: 179
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31474
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4098
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2847
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 1088
bin: 2.75e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3380
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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African
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BaseQRankSum
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FS
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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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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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 3.496503496503497e-3
allele num: 286
num of homozygotes: 0

African
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allele count: 41
allele frequency: 2.223427331887202e-2
allele num: 1844
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22016
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 5.767012687427913e-4
allele num: 1734
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7596
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1102
num of homozygotes: 0

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

VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.687e-1

MQRankSum
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SIO_000300: 3.22e-1

FS
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 16

GenotypeDepth
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variant carriers: 55

GenotypeDepth
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 1061

GenotypeDepth
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variant carriers: 8364

GenotypeDepth
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variant carriers: 7239

GenotypeDepth
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variant carriers: 26

GenotypeDepth
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variant carriers: 16

GenotypeDepth
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variant carriers: 41

GenotypeDepth
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variant carriers: 427

GenotypeDepth
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variant carriers: 2966

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 8

GenotypeDepth
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variant carriers: 15

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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variant carriers: 599

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 725

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 816

GenotypeQuality
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variant carriers: 350

South Asian
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allele count: 1420
allele frequency: 1.86940494997367e-1
allele num: 7596
num of homozygotes: 118

Other
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allele count: 110
allele frequency: 3.846153846153846e-1
allele num: 286
num of homozygotes: 17

Latino
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allele count: 589
allele frequency: 3.39677047289504e-1
allele num: 1734
num of homozygotes: 53

African
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allele count: 239
allele frequency: 1.296095444685466e-1
allele num: 1844
num of homozygotes: 10

European (Finnish)
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allele count: 556
allele frequency: 5.045372050816697e-1
allele num: 1102
num of homozygotes: 90

European (Non-Finnish)
type: Population
allele count: 11202
allele frequency: 5.088117732558139e-1
allele num: 22016
num of homozygotes: 2126

East Asian
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allele count: 297
allele frequency: 2.313084112149533e-1
allele num: 1284
num of homozygotes: 21

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 5.41347e5

VQSLOD
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SIO_000300: 3.4e0

MQRankSum
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SIO_000300: 3.22e-1

InbreedingCoeff
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SIO_000300: 1.687e-1

ClippingRankSum
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SIO_000300: -4.4e-2

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 1.689e1

GenotypeDepth
all individuals: 79
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 129
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.107e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

VQSLOD
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SIO_000300: -1.347e0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 5.5e-1

DP
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SIO_000300: 5.47102e5

ClippingRankSum
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SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 222
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.21017177500842e-5
allele num: 23752
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 5.5e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.216207100092756e-5
allele num: 23718
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23718
num of homozygotes: 0

European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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DP
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BaseQRankSum
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FS
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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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South Asian
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East Asian
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Other
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European (Finnish)
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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QD
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQRankSum
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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South Asian
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Latino
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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MQ
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VQSLOD
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FS
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DP
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East Asian
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European (Finnish)
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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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DP
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VQSLOD
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ReadPosRankSum
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MQ
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FS
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QD
type: SiteQuality
SIO_000300: 8.41e0

GenotypeDepth
all individuals: 5700
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 309
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12266
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1233
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6769
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6522
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4542
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5579
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 685
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4080
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.596863534997482e-5
allele num: 27802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7372
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.43e-2

DP
type: SiteQuality
SIO_000300: 6.20052e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.097e-1

QD
type: SiteQuality
SIO_000300: 7.08e0

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6487
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30063
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5998
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12286
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3123
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6315
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5841
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 8.857395925597874e-4
allele num: 2258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1506
num of homozygotes: 0