X-117727327-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117727327
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117727327
    reference: chr 0
allele count: 26464
allele frequency: 3.220914523569003e-1
allele num: 82163
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2263+27T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2263+27T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 6.25e1
  variant carriers: 1091
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 2250
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 1360
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 165
genotype depth: GenotypeDepth
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  variant carriers: 429
genotype depth: GenotypeDepth
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  variant carriers: 1114
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 1555
genotype depth: GenotypeDepth
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  variant carriers: 1970
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 858
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1763
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 1.25e1
  variant carriers: 1366
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 1636
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 2678
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 2582
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 2022
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 9.75e1
  variant carriers: 1180
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 291
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.25e1
  variant carriers: 596
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.25e1
  variant carriers: 201
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 573
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 100
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 486
genotype quality: GenotypeQuality
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  variant carriers: 857
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 569
genotype quality: GenotypeQuality
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  variant carriers: 351
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 341
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 861
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 786
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 170
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 2.25e1
  variant carriers: 572
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 735
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 1.25e1
  variant carriers: 211
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 625
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 5.75e1
  variant carriers: 434
genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 849
  bin: 4.25e1
  variant carriers: 349
genotype quality: GenotypeQuality
  all individuals: 10752
  bin: 6.25e1
  variant carriers: 822
num of homozygotes: 2746
population: Latino
  type: Population
  allele count: 1664
  allele frequency: 1.834417374049168e-1
  allele num: 9071
  num of homozygotes: 139
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

X-117727328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117727328
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117727328
    reference: chr 0
allele count: 1
allele frequency: 1.221851593905404e-5
allele num: 81843
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2263+28C>T
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2263+28C>T
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 390
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genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 11741
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2322
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.173676774263667e-5
  allele num: 46005
  num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-117727332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117727332
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117727332
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 81569
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2263+32A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2263+32A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3762
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9136
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

X-117727334-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117727334
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117727334
    reference: chr 0
allele count: 9
allele frequency: 1.105257340750838e-4
allele num: 81429
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2263+34T>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2263+34T>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6751
  num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

X-117727352-T-TCCAGGGTATA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117727352
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117727362
    reference: chr 0
allele count: 1
allele frequency: 1.250484562768073e-5
allele num: 79969
alternate allele: TCCAGGGTATA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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population: African
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population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
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site quality: VQSLOD
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site quality: FS
site quality: MQ
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X-117731344-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731344
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731345
    reference: chr 0
allele count: 2
allele frequency: 2.297081557880712e-5
allele num: 87067
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-50_2264-49insA
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-50_2264-49insA
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: South Asian
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  allele num: 9712
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population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
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X-117731344-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731344
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731344
    reference: chr 0
allele count: 1
allele frequency: 1.148540778940356e-5
allele num: 87067
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-50C>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-50C>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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population: Other
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population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
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site quality: FS
site quality: InbreedingCoeff
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site quality: ClippingRankSum
site quality: VQSLOD
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X-117731344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731344
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731344
    reference: chr 0
allele count: 1
allele frequency: 1.148540778940356e-5
allele num: 87067
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-50C>T
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-50C>T
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15618
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  variant carriers: 0
genotype depth: GenotypeDepth
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population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
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site quality: InbreedingCoeff
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X-117731346-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731346
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731346
    reference: chr 0
allele count: 1
allele frequency: 1.147894761008311e-5
allele num: 87116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-48G>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-48G>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: African
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population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
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reference allele: G
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site quality: FS
site quality: BaseQRankSum
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X-117731348-T-A
type: Variant
location: Region
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    reference: chr 0
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allele count: 2
allele frequency: 2.295341604214247e-5
allele num: 87133
alternate allele: A
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000147251
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  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-46T>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
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  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-46T>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Latino
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population: Other
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population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
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X-117731363-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731363
    reference: chr 0
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allele count: 2
allele frequency: 2.293025762144438e-5
allele num: 87221
alternate allele: A
annotation: Annotation
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  gene symbol: DOCK11
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  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
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  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-31C>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: European (Finnish)
population: East Asian
population: Other
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population: African
population: South Asian
reference allele: C
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X-117731369-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731369
    reference: chr 0
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    type: ExactPosition
    position: 24117731369
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allele count: 1
allele frequency: 1.14492454947219e-5
allele num: 87342
alternate allele: C
annotation: Annotation
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  ensembl gene: ENSG00000147251
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  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-25T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-25T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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X-117731376-T-A
type: Variant
location: Region
  begin: Position
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    reference: chr 0
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annotation: Annotation
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  gene symbol: DOCK11
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  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
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  gene symbol: DOCK11
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  variant of: http://identifiers.org/hgnc/23483
canonical: true
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6628
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

X-117731391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731391
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731391
    reference: chr 0
allele count: 1
allele frequency: 1.14105753212077e-5
allele num: 87638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2264-3C>T
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2264-3C>T
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 382
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genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 1357
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
hgvs: c.2264-3C>T
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9305
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

X-117731416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731416
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731416
    reference: chr 0
allele count: 2
allele frequency: 2.280371700587196e-5
allele num: 87705
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2286G>A
  hgvsp: ENST00000276204.6:c.2286G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2286G>A
  hgvsp: ENST00000276202.7:c.2286G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
hgvs: p.Leu762Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4527
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

X-117731434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731434
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731434
    reference: chr 0
allele count: 2
allele frequency: 2.280241705620796e-5
allele num: 87710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2304C>T
  hgvsp: ENST00000276204.6:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2304C>T
  hgvsp: ENST00000276202.7:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2848
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hgvs: p.Ile768Ile
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.084592774801443e-5
  allele num: 47971
  num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-117731440-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731440
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731440
    reference: chr 0
allele count: 1
allele frequency: 1.140172850204091e-5
allele num: 87706
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2310A>G
  hgvsp: ENST00000276202.7:c.2310A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2310A>G
  hgvsp: ENST00000276204.6:c.2310A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2849
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hgvs: p.Thr770Thr
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10123
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-117731460-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731460
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731460
    reference: chr 0
allele count: 1
allele frequency: 1.140224852340882e-5
allele num: 87702
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2330T>C
  hgvsp: ENSP00000276202.7:p.Val777Ala
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2330T>C
  hgvsp: ENSP00000276204.6:p.Val777Ala
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val777Ala
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4527
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

X-117731465-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731465
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731465
    reference: chr 0
allele count: 1
allele frequency: 1.140406897180914e-5
allele num: 87688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2335G>A
  hgvsp: ENSP00000276204.6:p.Ala779Thr
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2335G>A
  hgvsp: ENSP00000276202.7:p.Ala779Thr
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ala779Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4527
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-117731469-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731469
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731469
    reference: chr 0
allele count: 109
allele frequency: 1.243298733888445e-3
allele num: 87670
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2339A>G
  hgvsp: ENSP00000276202.7:p.Asn780Ser
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2339A>G
  hgvsp: ENSP00000276204.6:p.Asn780Ser
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2847
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hgvs: p.Asn780Ser
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8507
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-117731477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731477
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731477
    reference: chr 0
allele count: 43
allele frequency: 4.904644584359886e-4
allele num: 87672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2347C>T
  hgvsp: ENSP00000276204.6:p.Pro783Ser
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2347C>T
  hgvsp: ENSP00000276202.7:p.Pro783Ser
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Pro783Ser
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10118
  num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-117731482-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731482
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731482
    reference: chr 0
allele count: 1
allele frequency: 1.140849248180345e-5
allele num: 87654
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2352C>G
  hgvsp: ENST00000276202.7:c.2352C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2352C>G
  hgvsp: ENST00000276204.6:c.2352C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly784Gly
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 632
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

X-117731514-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731514
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731514
    reference: chr 0
allele count: 2
allele frequency: 2.286890400777543e-5
allele num: 87455
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2384G>C
  hgvsp: ENSP00000276204.6:p.Arg795Thr
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2384G>C
  hgvsp: ENSP00000276202.7:p.Arg795Thr
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg795Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

X-117731523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731523
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731523
    reference: chr 0
allele count: 1
allele frequency: 1.145396650860193e-5
allele num: 87306
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+8A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+8A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.2385+8A>G
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9275
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

X-117731532-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731532
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731532
    reference: chr 0
allele count: 1
allele frequency: 1.148105625717566e-5
allele num: 87100
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+17T>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+17T>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47669
  num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

X-117731540-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731540
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731540
    reference: chr 0
allele count: 1
allele frequency: 1.150258232973302e-5
allele num: 86937
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+25A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+25A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
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  allele frequency: 0.0e0
  allele num: 9250
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

X-117731545-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731545
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731545
    reference: chr 0
allele count: 12
allele frequency: 1.381994909652083e-4
allele num: 86831
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+30T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+30T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
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  allele num: 9236
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population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
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site quality: DP
site quality: MQRankSum
site quality: FS
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X-117731547-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731547
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731547
    reference: chr 0
allele count: 2
allele frequency: 2.304731614003549e-5
allele num: 86778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+32A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+32A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Latino
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  allele num: 9231
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population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
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site quality: VQSLOD

X-117731551-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731551
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731551
    reference: chr 0
allele count: 1
allele frequency: 1.153668666359022e-5
allele num: 86680
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+36T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+36T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  allele num: 6559
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population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
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site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
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X-117731557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731557
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731557
    reference: chr 0
allele count: 3
allele frequency: 3.468047720336632e-5
allele num: 86504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+42G>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+42G>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 2
  allele frequency: 3.055300947143294e-4
  allele num: 6546
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
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X-117731563-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731563
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731563
    reference: chr 0
allele count: 1
allele frequency: 1.157997128167122e-5
allele num: 86356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2385+48A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2385+48A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
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  allele num: 623
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
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site quality: VQSLOD
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site quality: FS
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X-117731944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731944
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731944
    reference: chr 0
allele count: 1
allele frequency: 1.190334483990001e-5
allele num: 84010
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2386-49A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2386-49A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
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  allele frequency: 0.0e0
  allele num: 9182
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

X-117731952-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731952
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731952
    reference: chr 0
allele count: 4
allele frequency: 4.750480986199853e-5
allele num: 84202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2386-41A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2386-41A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
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population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

X-117731953-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731953
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731953
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 84193
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2386-40T>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2386-40T>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 1.25e1
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genotype depth: GenotypeDepth
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  allele num: 8574
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
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population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
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site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP

X-117731954-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731954
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731954
    reference: chr 0
allele count: 1
allele frequency: 1.187775415424452e-5
allele num: 84191
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2386-39C>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2386-39C>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 1.538224888478696e-4
  allele num: 6501
  num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

X-117731956-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731956
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731956
    reference: chr 0
allele count: 1
allele frequency: 1.186084852510349e-5
allele num: 84311
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2386-37A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2386-37A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17584
  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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population: East Asian
  type: Population
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  allele num: 6513
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
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site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

X-117731959-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117731959
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117731959
    reference: chr 0
allele count: 1
allele frequency: 1.184581487360516e-5
allele num: 84418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2386-34A>T
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2386-34A>T
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  allele num: 4483
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population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

X-117732001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732001
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732001
    reference: chr 0
allele count: 3
allele frequency: 3.449703325514005e-5
allele num: 86964
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
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  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2394C>T
  hgvsp: ENST00000276202.7:c.2394C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2394C>T
  hgvsp: ENST00000276204.6:c.2394C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Asn798Asn
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.096787721211105e-5
  allele num: 47692
  num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
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site quality: MQ
site quality: QD

X-117732002-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732002
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732002
    reference: chr 0
allele count: 2
allele frequency: 2.298084546530467e-5
allele num: 87029
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2395G>A
  hgvsp: ENSP00000276204.6:p.Val799Met
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2395G>A
  hgvsp: ENSP00000276202.7:p.Val799Met
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val799Met
num of homozygotes: 0
population: South Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 9763
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
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site quality: InbreedingCoeff
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X-117732005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732005
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732005
    reference: chr 0
allele count: 1
allele frequency: 1.147618118594856e-5
allele num: 87137
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
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  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2398G>A
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  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2398G>A
  hgvsp: ENSP00000276202.7:p.Asp800Asn
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asp800Asn
num of homozygotes: 0
population: Latino
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  allele num: 9291
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population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
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X-117732023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732023
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732023
    reference: chr 0
allele count: 1
allele frequency: 1.144190942584499e-5
allele num: 87398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
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  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2416G>A
  hgvsp: ENSP00000276204.6:p.Gly806Ser
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
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  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2416G>A
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  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Finnish)
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population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
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reference allele: G
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site quality: QD
site quality: MQ
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X-117732026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732026
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732026
    reference: chr 0
allele count: 1
allele frequency: 1.143916082316201e-5
allele num: 87419
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2419G>A
  hgvsp: ENSP00000276202.7:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
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  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2419G>A
  hgvsp: ENSP00000276204.6:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: East Asian
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  allele num: 6622
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population: Other
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population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
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site quality: DP
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X-117732032-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732032
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732032
    reference: chr 0
allele count: 4
allele frequency: 4.574513100261891e-5
allele num: 87441
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2425C>T
  hgvsp: ENSP00000276204.6:p.Pro809Ser
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2425C>T
  hgvsp: ENSP00000276202.7:p.Pro809Ser
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Pro809Ser
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 3
  allele frequency: 6.269592476489028e-5
  allele num: 47850
  num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
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X-117732037-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732037
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732037
    reference: chr 0
allele count: 2
allele frequency: 2.287282708142727e-5
allele num: 87440
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2430G>T
  hgvsp: ENSP00000276202.7:p.Leu810Phe
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2430G>T
  hgvsp: ENSP00000276204.6:p.Leu810Phe
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu810Phe
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8510
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
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site quality: MQ
site quality: FS
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X-117732038-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732038
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732038
    reference: chr 0
allele count: 1
allele frequency: 1.143628275065473e-5
allele num: 87441
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2431T>C
  hgvsp: ENST00000276202.7:c.2431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2431T>C
  hgvsp: ENST00000276204.6:c.2431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Leu811Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4518
  num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

X-117732043-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732043
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732043
    reference: chr 0
allele count: 7
allele frequency: 8.006313550113804e-5
allele num: 87431
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2436G>C
  hgvsp: ENSP00000276204.6:p.Lys812Asn
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2436G>C
  hgvsp: ENSP00000276202.7:p.Lys812Asn
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
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  variant carriers: 0
genotype depth: GenotypeDepth
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hgvs: p.Lys812Asn
num of homozygotes: 0
population: African
  type: Population
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  allele frequency: 0.0e0
  allele num: 8507
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
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population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
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site quality: InbreedingCoeff
site quality: FS
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site quality: QD
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X-117732044-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732044
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732044
    reference: chr 0
allele count: 5654
allele frequency: 6.467479581798632e-2
allele num: 87422
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2437A>T
  hgvsp: ENSP00000276202.7:p.Ile813Phe
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2437A>T
  hgvsp: ENSP00000276204.6:p.Ile813Phe
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 8.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 8.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 5160
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 5591
  bin: 6.75e1
  variant carriers: 35
hgvs: p.Ile813Phe
num of homozygotes: 134
population: European (Finnish)
  type: Population
  allele count: 522
  allele frequency: 1.155890168290523e-1
  allele num: 4516
  num of homozygotes: 15
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

X-117732052-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732052
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732052
    reference: chr 0
allele count: 1
allele frequency: 1.144872117784444e-5
allele num: 87346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2445C>A
  hgvsp: ENSP00000276204.6:p.Ser815Arg
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2445C>A
  hgvsp: ENSP00000276202.7:p.Ser815Arg
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser815Arg
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 628
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

X-117732077-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732077
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732077
    reference: chr 0
allele count: 1
allele frequency: 1.152990280291937e-5
allele num: 86731
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2470C>G
  hgvsp: ENSP00000276202.7:p.Gln824Glu
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2470C>G
  hgvsp: ENSP00000276204.6:p.Gln824Glu
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 326
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 342
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2010
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln824Glu
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: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

X-117732091-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117732091
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117732091
    reference: chr 0
allele count: 1
allele frequency: 1.164578189779662e-5
allele num: 85868
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2472+12C>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2472+12C>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1172
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6577
  num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

X-117733056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733056
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733056
    reference: chr 0
allele count: 166
allele frequency: 1.959372528652872e-3
allele num: 84721
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-46G>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-46G>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 341
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1925
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  variant carriers: 9
num of homozygotes: 2
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.089443294476523e-4
  allele num: 9179
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

X-117733076-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733076
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733077
    reference: chr 0
allele count: 1
allele frequency: 1.173103092299751e-5
allele num: 85244
alternate allele: TA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-25dupA
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-25dupA
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6536
  num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

X-117733077-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733077
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733077
    reference: chr 0
allele count: 2
allele frequency: 2.345160760770151e-5
allele num: 85282
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-25A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-25A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 1
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46851
  num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

X-117733078-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733078
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733078
    reference: chr 0
allele count: 1
allele frequency: 1.171659890566966e-5
allele num: 85349
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-24T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-24T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
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  allele num: 8434
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population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

X-117733079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733079
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733079
    reference: chr 0
allele count: 4
allele frequency: 4.684883053606774e-5
allele num: 85381
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-23G>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-23G>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
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  allele num: 9216
  num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

X-117733084-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733084
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733084
    reference: chr 0
allele count: 18
allele frequency: 2.102705481052287e-4
allele num: 85604
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-18T>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-18T>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 12
  allele frequency: 2.553517470315359e-4
  allele num: 46994
  num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
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X-117733084-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733084
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733084
    reference: chr 0
allele count: 1
allele frequency: 1.168169711695715e-5
allele num: 85604
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2473-18T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2473-18T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
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  allele num: 8438
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population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: QD
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X-117733109-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733109
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733109
    reference: chr 0
allele count: 11
allele frequency: 1.265269502404012e-4
allele num: 86938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2480A>C
  hgvsp: ENSP00000276204.6:p.His827Pro
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2480A>C
  hgvsp: ENSP00000276202.7:p.His827Pro
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.His827Pro
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
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  allele num: 47577
  num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
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X-117733110-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733110
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733110
    reference: chr 0
allele count: 1
allele frequency: 1.150099483605332e-5
allele num: 86949
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2481T>C
  hgvsp: ENST00000276202.7:c.2481T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2481T>C
  hgvsp: ENST00000276204.6:c.2481T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.His827His
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population: African
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  allele num: 8482
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population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
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site quality: FS
site quality: QD
site quality: ReadPosRankSum
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X-117733113-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733113
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733113
    reference: chr 0
allele count: 165
allele frequency: 1.896638925927629e-3
allele num: 86996
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2484G>A
  hgvsp: ENST00000276202.7:c.2484G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2484G>A
  hgvsp: ENST00000276204.6:c.2484G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val828Val
num of homozygotes: 1
population: African
  type: Population
  allele count: 9
  allele frequency: 1.061070502240038e-3
  allele num: 8482
  num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD

X-117733115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733115
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733115
    reference: chr 0
allele count: 1
allele frequency: 1.149200730891665e-5
allele num: 87017
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2486A>G
  hgvsp: ENSP00000276202.7:p.His829Arg
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2486A>G
  hgvsp: ENSP00000276204.6:p.His829Arg
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.His829Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9271
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-117733122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733122
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733122
    reference: chr 0
allele count: 1
allele frequency: 1.148712293518965e-5
allele num: 87054
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2493C>T
  hgvsp: ENST00000276202.7:c.2493C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2493C>T
  hgvsp: ENST00000276204.6:c.2493C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Phe831Phe
num of homozygotes: 0
population: Other
  type: Population
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  allele frequency: 0.0e0
  allele num: 626
  num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

X-117733128-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733128
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733128
    reference: chr 0
allele count: 1
allele frequency: 1.148712293518965e-5
allele num: 87054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2499T>A
  hgvsp: ENSP00000276204.6:p.His833Gln
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2499T>A
  hgvsp: ENSP00000276202.7:p.His833Gln
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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hgvs: p.His833Gln
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4505
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
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site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

X-117733129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733129
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733129
    reference: chr 0
allele count: 1
allele frequency: 1.148633126579371e-5
allele num: 87060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2500C>T
  hgvsp: ENSP00000276204.6:p.His834Tyr
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2500C>T
  hgvsp: ENSP00000276202.7:p.His834Tyr
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
hgvs: p.His834Tyr
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 627
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

X-117733140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733140
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733140
    reference: chr 0
allele count: 1
allele frequency: 1.150073029637382e-5
allele num: 86951
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2511G>A
  hgvsp: ENST00000276204.6:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2511G>A
  hgvsp: ENST00000276202.7:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu837Leu
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6587
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
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site quality: BaseQRankSum

X-117733152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733152
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733152
    reference: chr 0
allele count: 1
allele frequency: 1.154574423867362e-5
allele num: 86612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2523C>T
  hgvsp: ENST00000276204.6:c.2523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2523C>T
  hgvsp: ENST00000276202.7:c.2523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gly841Gly
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6575
  num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

X-117733154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733154
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733154
    reference: chr 0
allele count: 181
allele frequency: 2.091905136147196e-3
allele num: 86524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2525C>T
  hgvsp: ENSP00000276204.6:p.Ser842Leu
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2525C>T
  hgvsp: ENSP00000276202.7:p.Ser842Leu
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser842Leu
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6571
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

X-117733155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733155
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733155
    reference: chr 0
allele count: 1
allele frequency: 1.156430330854718e-5
allele num: 86473
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2526G>A
  hgvsp: ENST00000276202.7:c.2526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2526G>A
  hgvsp: ENST00000276204.6:c.2526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser842Ser
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 627
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

X-117733166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733166
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733166
    reference: chr 0
allele count: 1
allele frequency: 1.171261917590011e-5
allele num: 85378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2537C>T
  hgvsp: ENSP00000276204.6:p.Pro846Leu
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2537C>T
  hgvsp: ENSP00000276202.7:p.Pro846Leu
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro846Leu
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8350
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-117733172-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733172
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733172
    reference: chr 0
allele count: 7
allele frequency: 8.274916364238175e-5
allele num: 84593
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2543A>G
  hgvsp: ENSP00000276202.7:p.Glu848Gly
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2543A>G
  hgvsp: ENSP00000276204.6:p.Glu848Gly
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23014
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Glu848Gly
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 5
  allele frequency: 1.081970051068986e-4
  allele num: 46212
  num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff

X-117733173-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733173
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733173
    reference: chr 0
allele count: 5
allele frequency: 5.912541683418868e-5
allele num: 84566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2544G>T
  hgvsp: ENSP00000276204.6:p.Glu848Asp
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2544G>T
  hgvsp: ENSP00000276202.7:p.Glu848Asp
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Glu848Asp
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4399
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

X-117733176-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733176
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733176
    reference: chr 0
allele count: 10
allele frequency: 1.18923033013034e-4
allele num: 84088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2547C>G
  hgvsp: ENST00000276204.6:c.2547C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2547C>G
  hgvsp: ENST00000276202.7:c.2547C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 515
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  variant carriers: 0
hgvs: p.Leu849Leu
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 10
  allele frequency: 2.177890060109766e-4
  allele num: 45916
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

X-117733176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733176
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733176
    reference: chr 0
allele count: 2
allele frequency: 2.378460660260679e-5
allele num: 84088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2547C>T
  hgvsp: ENST00000276204.6:c.2547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2547C>T
  hgvsp: ENST00000276202.7:c.2547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu849Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4380
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
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site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
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X-117733192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733192
    reference: chr 0
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    type: ExactPosition
    position: 24117733192
    reference: chr 0
allele count: 1
allele frequency: 1.231572595046615e-5
allele num: 81197
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2562+1G>A
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2562+1G>A
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.2562+1G>A
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8910
  num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
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site quality: MQ
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X-117733195-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733195
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733195
    reference: chr 0
allele count: 1
allele frequency: 1.247831892087498e-5
allele num: 80139
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2562+4A>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2562+4A>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.2562+4A>C
num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele num: 4187
  num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

X-117733197-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733197
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733197
    reference: chr 0
allele count: 1
allele frequency: 1.251501802162595e-5
allele num: 79904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2562+6T>C
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2562+6T>C
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13622
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.2562+6T>C
num of homozygotes: 0
population: African
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  allele frequency: 0.0e0
  allele num: 7980
  num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

X-117733200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733200
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733200
    reference: chr 0
allele count: 2
allele frequency: 2.526560466908374e-5
allele num: 79159
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2562+9A>G
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2562+9A>G
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2188
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 956
  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 298
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 27041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8740
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

X-117733201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117733201
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117733201
    reference: chr 0
allele count: 1
allele frequency: 1.273009649413143e-5
allele num: 78554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276204
  ensembl transcript: ENST00000276204
  gene symbol: DOCK11
  hgvsc: ENST00000276204.6:c.2562+10C>T
  variant of: http://identifiers.org/hgnc/23483
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147251
  ensembl protein: ENSP00000276202
  ensembl transcript: ENST00000276202
  gene symbol: DOCK11
  hgvsc: ENST00000276202.7:c.2562+10C>T
  variant of: http://identifiers.org/hgnc/23483
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 10855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

African
type: Population
allele count: 1133
allele frequency: 1.374666343120602e-1
allele num: 8242
num of homozygotes: 56

East Asian
type: Population
allele count: 1453
allele frequency: 2.252363974577585e-1
allele num: 6451
num of homozygotes: 110

South Asian
type: Population
allele count: 3229
allele frequency: 4.393197278911565e-1
allele num: 7350
num of homozygotes: 320

European (Finnish)
type: Population
allele count: 1660
allele frequency: 3.728661275831087e-1
allele num: 4452
num of homozygotes: 157

European (Non-Finnish)
type: Population
allele count: 17125
allele frequency: 3.721450768194363e-1
allele num: 46017
num of homozygotes: 1947

Other
type: Population
allele count: 200
allele frequency: 3.448275862068966e-1
allele num: 580
num of homozygotes: 17

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.575e-1

DP
type: SiteQuality
SIO_000300: 2.090938e6

FS
type: SiteQuality
SIO_000300: 6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 2.369e1

VQSLOD
type: SiteQuality
SIO_000300: 4.028e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 583
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9145
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6469
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6937
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

QD
type: SiteQuality
SIO_000300: 2.831e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.398e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.6e-2

DP
type: SiteQuality
SIO_000300: 1.800978e6

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45915
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8181
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.894e1

DP
type: SiteQuality
SIO_000300: 1.773692e6

Latino
type: Population
allele count: 2
allele frequency: 2.189621195533173e-4
allele num: 9134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.225340031858841e-4
allele num: 8161
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6459
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.308500894142278e-4
allele num: 45854
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.104e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

FS
type: SiteQuality
SIO_000300: 2.361e0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

QD
type: SiteQuality
SIO_000300: 1.491e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

DP
type: SiteQuality
SIO_000300: 1.763688e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6213
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9100
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.562011871290222e-4
allele num: 6402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4472
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.013e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.211e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

FS
type: SiteQuality
SIO_000300: 3.332e0

MQ
type: SiteQuality
SIO_000300: 5.487e1

QD
type: SiteQuality
SIO_000300: 5.14e0

DP
type: SiteQuality
SIO_000300: 1.706883e6

MQRankSum
type: SiteQuality
SIO_000300: -2.441e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.106e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8505
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.152852529601722e-4
allele num: 9290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

DP
type: SiteQuality
SIO_000300: 2.318772e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

QD
type: SiteQuality
SIO_000300: 2.128e1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.076426264800861e-4
allele num: 9290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

DP
type: SiteQuality
SIO_000300: 2.318772e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 2.128e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47786
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

QD
type: SiteQuality
SIO_000300: 2.128e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

DP
type: SiteQuality
SIO_000300: 2.318772e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9747
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.09209397686144e-5
allele num: 47799
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 1.144e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.036e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 2.319837e6

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.288e0

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.748e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8505
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6619
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47807
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.049600327936052e-4
allele num: 9758
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 2.320831e6

FS
type: SiteQuality
SIO_000300: 7.666e0

VQSLOD
type: SiteQuality
SIO_000300: -1.423e0

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

QD
type: SiteQuality
SIO_000300: 2.044e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.75e-2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

DP
type: SiteQuality
SIO_000300: 2.333973e6

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-1

FS
type: SiteQuality
SIO_000300: 5.044e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.148e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 5.983e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47861
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.004e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.811e1

DP
type: SiteQuality
SIO_000300: 2.339424e6

FS
type: SiteQuality
SIO_000300: 7.74e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

European (Non-Finnish)
type: Population
allele count: 76
allele frequency: 1.587069559588197e-3
allele num: 47887
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.700904924197908e-4
allele num: 8509
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.416961130742049e-4
allele num: 4528
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 6.455083378160301e-4
allele num: 9295
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.876e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.686e-1

DP
type: SiteQuality
SIO_000300: 2.349848e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

QD
type: SiteQuality
SIO_000300: 1.649e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085766727849157e-5
allele num: 47944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 2.348898e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.51e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 2.852e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.401e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47971
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.014772384684956e-4
allele num: 6634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.249e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-3

DP
type: SiteQuality
SIO_000300: 2.351269e6

VQSLOD
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 5.905e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 1.094e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.696e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

South Asian
type: Population
allele count: 1
allele frequency: 9.878494517435543e-5
allele num: 10123
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.79e-1

DP
type: SiteQuality
SIO_000300: 2.351044e6

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 5.335e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.442e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.074460083807887e-4
allele num: 9307
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47971
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 2.033e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 2.350811e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
type: SiteQuality
SIO_000300: 1.435e1

South Asian
type: Population
allele count: 1
allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47967
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e0

VQSLOD
type: SiteQuality
SIO_000300: -3.232e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.91e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.350174e6

QD
type: SiteQuality
SIO_000300: 2.896e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.361e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.880446596186147e-5
allele num: 10121
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.773e1

VQSLOD
type: SiteQuality
SIO_000300: -1.046e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.62e-2

QD
type: SiteQuality
SIO_000300: 2.864e1

DP
type: SiteQuality
SIO_000300: 2.349936e6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.976479889317126e-4
allele num: 10119
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085331776285607e-5
allele num: 47954
num of homozygotes: 0

East Asian
type: Population
allele count: 106
allele frequency: 1.59975852701479e-2
allele num: 6626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9305
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.884e-1

FS
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e0

MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

DP
type: SiteQuality
SIO_000300: 2.355139e6

VQSLOD
type: SiteQuality
SIO_000300: 1.982e1

QD
type: SiteQuality
SIO_000300: 1.727e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e-1

African
type: Population
allele count: 38
allele frequency: 4.467434751939807e-3
allele num: 8506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.224419604471195e-4
allele num: 9304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.170837504170838e-5
allele num: 47952
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.705e0

QD
type: SiteQuality
SIO_000300: 1.582e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 2.616e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.149e-1

DP
type: SiteQuality
SIO_000300: 2.347622e6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47937
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9301
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.882399446585631e-5
allele num: 10119
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 2.343286e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 3.245e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10087
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.025260928755105e-4
allele num: 6611
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8491
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47825
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

DP
type: SiteQuality
SIO_000300: 2.335061e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.806e0

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.975e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093626999413784e-5
allele num: 47764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 3.903e0

DP
type: SiteQuality
SIO_000300: 2.326807e6

VQSLOD
type: SiteQuality
SIO_000300: -2.391e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.91e0

QD
type: SiteQuality
SIO_000300: 1.782e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8435
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.000100010001e-4
allele num: 9999
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9259
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.308627e6

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 3.441e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.003109639883639e-4
allele num: 9969
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.27e-2

DP
type: SiteQuality
SIO_000300: 2.28115e6

MQRankSum
type: SiteQuality
SIO_000300: -1.677e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.832e0

QD
type: SiteQuality
SIO_000300: 2.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.695e0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.313159776254363e-4
allele num: 47554
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.192037191560377e-4
allele num: 8389
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.602e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.832e1

DP
type: SiteQuality
SIO_000300: 2.258987e6

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 2.124e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

African
type: Population
allele count: 2
allele frequency: 2.384642899725766e-4
allele num: 8387
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6569
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.2399e1

QD
type: SiteQuality
SIO_000300: 1.189e1

DP
type: SiteQuality
SIO_000300: 2.238877e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

MQRankSum
type: SiteQuality
SIO_000300: 8.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.655e0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4507
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47470
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9929
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Other
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.139e0

QD
type: SiteQuality
SIO_000300: 1.451e1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.81e0

MQ
type: SiteQuality
SIO_000300: 5.784e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

FS
type: SiteQuality
SIO_000300: 2.331e0

VQSLOD
type: SiteQuality
SIO_000300: -2.189e0

DP
type: SiteQuality
SIO_000300: 2.217976e6

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47391
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8346
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Latino
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allele frequency: 1.085894233901618e-4
allele num: 9209
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South Asian
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allele frequency: 0.0e0
allele num: 9884
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4502
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Other
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allele frequency: 0.0e0
allele num: 626
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VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.9e-1

DP
type: SiteQuality
SIO_000300: 2.185949e6

QD
type: SiteQuality
SIO_000300: 1.439e1

Latino
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allele frequency: 0.0e0
allele num: 9206
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4497
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East Asian
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allele count: 1
allele frequency: 1.529987760097919e-4
allele num: 6536
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8320
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9849
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47325
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 2.162369e6

FS
type: SiteQuality
SIO_000300: 2.246e0

MQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

QD
type: SiteQuality
SIO_000300: 1.087e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.15368711233632e-5
allele num: 46432
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 601
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8316
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4470
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.479e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.371e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.771278e6

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46536
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9189
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6500
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4478
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.67e0

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.802924e6

QD
type: SiteQuality
SIO_000300: 1.782e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46523
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 6501
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4480
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 3.027e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.654e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.807351e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8333
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9191
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8555
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46533
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.81327e6

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.92e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4481
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.147166813389732e-5
allele num: 46573
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MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

QD
type: SiteQuality
SIO_000300: 1.661e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

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
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allele num: 6525
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Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8639
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.144864122857817e-5
allele num: 46623
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Other
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

MQ
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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African
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allele count: 2
allele frequency: 2.353494939985879e-4
allele num: 8498
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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Latino
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allele count: 0
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East Asian
type: Population
allele count: 0
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Other
type: Population
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
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Other
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allele count: 0
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allele num: 628
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47711
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Latino
type: Population
allele count: 1
allele frequency: 1.076310407921645e-4
allele num: 9291
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African
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allele count: 1
allele frequency: 1.176747469992939e-4
allele num: 8498
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East Asian
type: Population
allele count: 0
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allele num: 6621
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 1.239e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

MQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

DP
type: SiteQuality
SIO_000300: 1.932238e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47746
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4517
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East Asian
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allele count: 1
allele frequency: 1.510117789187557e-4
allele num: 6622
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Other
type: Population
allele count: 0
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African
type: Population
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South Asian
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allele count: 0
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.35e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.927e1

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

DP
type: SiteQuality
SIO_000300: 1.934472e6

QD
type: SiteQuality
SIO_000300: 1.209e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9299
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.090825457890775e-5
allele num: 47828
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African
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allele count: 0
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East Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
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South Asian
type: Population
allele count: 0
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.871e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

Other
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allele count: 0
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num of homozygotes: 0

South Asian
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allele count: 0
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Latino
type: Population
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47841
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African
type: Population
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FS
type: SiteQuality
SIO_000300: 1.0923e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.941644e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.141e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

VQSLOD
type: SiteQuality
SIO_000300: -1.814e0

African
type: Population
allele count: 0
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allele num: 8510
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South Asian
type: Population
allele count: 1
allele frequency: 9.987016878058524e-5
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

Latino
type: Population
allele count: 0
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allele num: 9299
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 1.101e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.46e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.141e0

QD
type: SiteQuality
SIO_000300: 1.251e1

DP
type: SiteQuality
SIO_000300: 1.942259e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.179815670128947e-5
allele num: 47849
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9299
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10015
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.033e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.809999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.353e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 1.942352e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.985022466300549e-5
allele num: 10015
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47849
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9299
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.62e-1

FS
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

DP
type: SiteQuality
SIO_000300: 1.942307e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9297
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10017
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.463210702341137e-4
allele num: 47840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.74e-1

DP
type: SiteQuality
SIO_000300: 1.942417e6

MQ
type: SiteQuality
SIO_000300: 5.926e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.379999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.114e0

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

QD
type: SiteQuality
SIO_000300: 1.596e1

VQSLOD
type: SiteQuality
SIO_000300: -1.938e-1

Latino
type: Population
allele count: 170
allele frequency: 1.828743545611015e-2
allele num: 9296
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.020691738408096e-4
allele num: 6621
num of homozygotes: 0

Other
type: Population
allele count: 52
allele frequency: 8.253968253968254e-2
allele num: 630
num of homozygotes: 3

African
type: Population
allele count: 543
allele frequency: 6.385230479774225e-2
allele num: 8504
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 4100
allele frequency: 8.571129925786558e-2
allele num: 47835
num of homozygotes: 103

South Asian
type: Population
allele count: 265
allele frequency: 2.644710578842316e-2
allele num: 10020
num of homozygotes: 1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.534e-1

QD
type: SiteQuality
SIO_000300: 1.787e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.295825e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.953e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

Latino
type: Population
allele count: 1
allele frequency: 1.075847229693384e-4
allele num: 9295
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 2.634e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.284e0

VQSLOD
type: SiteQuality
SIO_000300: -1.068e0

DP
type: SiteQuality
SIO_000300: 1.94389e6

QD
type: SiteQuality
SIO_000300: 6.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.101723413198823e-5
allele num: 47580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8459
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6615
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4505
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9671
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.222e0

MQRankSum
type: SiteQuality
SIO_000300: 6.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.537e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

VQSLOD
type: SiteQuality
SIO_000300: -4.325e0

DP
type: SiteQuality
SIO_000300: 1.921061e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.4e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8389
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.11999152003392e-5
allele num: 47170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.216e1

DP
type: SiteQuality
SIO_000300: 1.880864e6

MQ
type: SiteQuality
SIO_000300: 5.725e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.589e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46571
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

South Asian
type: Population
allele count: 165
allele frequency: 1.827647319450598e-2
allele num: 9028
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.596e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.535e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.492e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

DP
type: SiteQuality
SIO_000300: 1.483385e6

African
type: Population
allele count: 1
allele frequency: 1.186098920649982e-4
allele num: 8431
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9209
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

FS
type: SiteQuality
SIO_000300: 4.218e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

QD
type: SiteQuality
SIO_000300: 1.224e1

DP
type: SiteQuality
SIO_000300: 1.553952e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.170609941393532e-4
allele num: 9214
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4451
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.916e1

VQSLOD
type: SiteQuality
SIO_000300: -3.501e0

QD
type: SiteQuality
SIO_000300: 3.478e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.74e-1

DP
type: SiteQuality
SIO_000300: 1.558597e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.187e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

South Asian
type: Population
allele count: 1
allele frequency: 1.085776330076004e-4
allele num: 9210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4455
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46881
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.97e1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-2

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.562975e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8433
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46897
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.338394793926247e-4
allele num: 9220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.748e0

VQSLOD
type: SiteQuality
SIO_000300: -1.526e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 1.568559e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.933e1

Latino
type: Population
allele count: 6
allele frequency: 6.501950585175553e-4
allele num: 9228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6553
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4463
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

FS
type: SiteQuality
SIO_000300: 2.9315e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.066e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.43e0

DP
type: SiteQuality
SIO_000300: 1.586728e6

QD
type: SiteQuality
SIO_000300: 1.417e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.191e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6553
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4463
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.43e0

DP
type: SiteQuality
SIO_000300: 1.586728e6

QD
type: SiteQuality
SIO_000300: 1.417e1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.066e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.191e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

FS
type: SiteQuality
SIO_000300: 2.9315e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9269
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.443457009553433e-4
allele num: 4501
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.769e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.480000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.07e-1

DP
type: SiteQuality
SIO_000300: 1.639447e6

QD
type: SiteQuality
SIO_000300: 1.336e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9267
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9895
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.101590904314566e-5
allele num: 47583
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4501
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.814e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.91e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

MQ
type: SiteQuality
SIO_000300: 5.837e1

VQSLOD
type: SiteQuality
SIO_000300: -1.489e0

DP
type: SiteQuality
SIO_000300: 1.639873e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

Other
type: Population
allele count: 2
allele frequency: 3.2e-3
allele num: 625
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.394325169921243e-4
allele num: 9269
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 123
allele frequency: 2.583925045166169e-3
allele num: 47602
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.554174067495559e-3
allele num: 4504
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.915515676983567e-3
allele num: 9919
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.876e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.105e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 3.067e1

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

DP
type: SiteQuality
SIO_000300: 1.647546e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.642e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6597
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8485
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47615
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South Asian
type: Population
allele count: 1
allele frequency: 1.008064516129032e-4
allele num: 9920
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.64221e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

FS
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.081e0

QD
type: SiteQuality
SIO_000300: 1.213e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47629
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.005935016597928e-4
allele num: 9941
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 2.838e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.53e-2

DP
type: SiteQuality
SIO_000300: 1.644376e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.100222623598102e-5
allele num: 47614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8483
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9957
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9273
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.53e-2

DP
type: SiteQuality
SIO_000300: 1.645289e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.85e-1

QD
type: SiteQuality
SIO_000300: 2.913e1

VQSLOD
type: SiteQuality
SIO_000300: -2.303e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

South Asian
type: Population
allele count: 1
allele frequency: 1.004116879204739e-4
allele num: 9959
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8485
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9273
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 1.645839e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.117e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.31e-1

FS
type: SiteQuality
SIO_000300: 7.992e0

QD
type: SiteQuality
SIO_000300: 1.057e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4505
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.103403306549998e-5
allele num: 47542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9267
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
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MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

FS
type: SiteQuality
SIO_000300: 2.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 1.067e1

DP
type: SiteQuality
SIO_000300: 1.645111e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.080497028633171e-4
allele num: 9255
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9871
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MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.69e-2

DP
type: SiteQuality
SIO_000300: 1.637196e6

QD
type: SiteQuality
SIO_000300: 1.907e1

VQSLOD
type: SiteQuality
SIO_000300: -5.837e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e0

FS
type: SiteQuality
SIO_000300: 9.917999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

African
type: Population
allele count: 6
allele frequency: 7.098071690524074e-4
allele num: 8453
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 136
allele frequency: 2.876723919113292e-3
allele num: 47276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 8.916629514043691e-4
allele num: 4486
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.594896331738437e-3
allele num: 627
num of homozygotes: 0

South Asian
type: Population
allele count: 29
allele frequency: 2.941773179143843e-3
allele num: 9858
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.403652869339674e-4
allele num: 9253
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.717e-1

QD
type: SiteQuality
SIO_000300: 1.68e1

VQSLOD
type: SiteQuality
SIO_000300: 2.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 1.640412e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4485
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9253
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.5220700152207e-4
allele num: 6570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8453
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9847
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47238
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

DP
type: SiteQuality
SIO_000300: 1.633074e6

FS
type: SiteQuality
SIO_000300: 1.0088e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.76e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
type: SiteQuality
SIO_000300: 1.636e1

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.816e-1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.143576772202096e-5
allele num: 46651
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4445
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9211
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6493
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9611
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DP
type: SiteQuality
SIO_000300: 1.600548e6

FS
type: SiteQuality
SIO_000300: 5.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.368e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.916e0

QD
type: SiteQuality
SIO_000300: 2.316e1

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.04e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8283
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
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European (Finnish)
type: Population
allele count: 2
allele frequency: 4.541326067211626e-4
allele num: 4404
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South Asian
type: Population
allele count: 0
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MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.526e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

DP
type: SiteQuality
SIO_000300: 1.575277e6

FS
type: SiteQuality
SIO_000300: 5.81e-1

QD
type: SiteQuality
SIO_000300: 1.867e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.99e-2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9171
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46198
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 6.039376736320811e-4
allele num: 8279
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: 6436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
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MQRankSum
type: SiteQuality
SIO_000300: -6.49e-1

QD
type: SiteQuality
SIO_000300: 1.715e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.217e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.38e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

DP
type: SiteQuality
SIO_000300: 1.575303e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9395
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8239
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9145
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
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MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.561054e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

QD
type: SiteQuality
SIO_000300: 1.858e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9145
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.355780120219531e-5
allele num: 45916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8239
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9395
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-2

QD
type: SiteQuality
SIO_000300: 1.858e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

DP
type: SiteQuality
SIO_000300: 1.561054e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8075
num of homozygotes: 0

South Asian
type: Population
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: 589
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4241
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44302
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.618384851917786e-4
allele num: 6179
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.946999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.572e-1

QD
type: SiteQuality
SIO_000300: 1.127e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.012e0

DP
type: SiteQuality
SIO_000300: 1.461857e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6101
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43721
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.144033863402357e-4
allele num: 8741
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7991
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.418008e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

QD
type: SiteQuality
SIO_000300: 1.865e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 579
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4179
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6075
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43584
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.147973826196763e-4
allele num: 8711
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.535e-1

DP
type: SiteQuality
SIO_000300: 1.40846e6

QD
type: SiteQuality
SIO_000300: 2.85e1

African
type: Population
allele count: 2
allele frequency: 2.519208968383928e-4
allele num: 7939
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8597
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4161
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.374297e6

VQSLOD
type: SiteQuality
SIO_000300: 3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.017e1