8-12285049-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285049
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285049
    reference: chr 8
allele count: 3
allele frequency: 1.342882721575649e-3
allele num: 2234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+117T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+117T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.325T>C
  hgvsp: ENSP00000377318.3:p.Tyr109His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+117T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+117T>C
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22502
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21392
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7790
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
hgvs: p.Tyr109His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

8-12285056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285056
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285056
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 2944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+110C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+110C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+110C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.318C>T
  hgvsp: ENST00000393715.3:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+110C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10435
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9468
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu106Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-12285063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285063
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285063
    reference: chr 8
allele count: 1
allele frequency: 2.632964718272775e-4
allele num: 3798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+103C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.311C>T
  hgvsp: ENSP00000377318.3:p.Ser104Phe
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+103C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+103C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+103C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11862
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 710
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser104Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-12285064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285064
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285064
    reference: chr 8
allele count: 4057
allele frequency: 4.478913667476264e-1
allele num: 9058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+102T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.310T>C
  hgvsp: ENSP00000377318.3:p.Ser104Pro
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+102T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+102T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+102T>C
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17222
  bin: 2.5e0
  variant carriers: 1656
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.25e1
  variant carriers: 349
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 7.5e0
  variant carriers: 4052
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 1.25e1
  variant carriers: 2298
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.75e1
  variant carriers: 162
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.75e1
  variant carriers: 983
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 8.25e1
  variant carriers: 331
genotype quality: GenotypeQuality
  all individuals: 3323
  bin: 2.5e0
  variant carriers: 152
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 8.75e1
  variant carriers: 124
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 3.25e1
  variant carriers: 379
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 1.75e1
  variant carriers: 1017
genotype quality: GenotypeQuality
  all individuals: 15246
  bin: 7.5e0
  variant carriers: 985
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 5.25e1
  variant carriers: 478
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 5.75e1
  variant carriers: 604
genotype quality: GenotypeQuality
  all individuals: 5421
  bin: 2.25e1
  variant carriers: 460
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 168
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 6.75e1
  variant carriers: 187
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.25e1
  variant carriers: 242
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 373
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 2.75e1
  variant carriers: 314
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 1.25e1
  variant carriers: 922
hgvs: p.Ser104Pro
num of homozygotes: 255
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

8-12285074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285074
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285074
    reference: chr 8
allele count: 6
allele frequency: 5.658242172764995e-4
allele num: 10604
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+92G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+92G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+92G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.300G>A
  hgvsp: ENST00000393715.3:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+92G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18673
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12975
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1558
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17278
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Lys100Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

8-12285076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285076
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285076
    reference: chr 8
allele count: 10
allele frequency: 9.257544899092761e-4
allele num: 10802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+90A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+90A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+90A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+90A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.298A>G
  hgvsp: ENSP00000377318.3:p.Lys100Glu
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18449
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13351
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17154
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11052
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 6.25e1
  variant carriers: 1
hgvs: p.Lys100Glu
num of homozygotes: 2
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-12285083-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285083
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285083
    reference: chr 8
allele count: 177
allele frequency: 1.52955409609402e-2
allele num: 11572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+83T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+83T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.291T>C
  hgvsp: ENST00000393715.3:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+83T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+83T>C
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14856
  bin: 7.5e0
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 1.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 2.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16802
  bin: 2.5e0
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 2.5e0
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 6.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 12370
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 8.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 1.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 6.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 3.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 3.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 15594
  bin: 7.5e0
  variant carriers: 119
hgvs: p.Ala97Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

8-12285085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285085
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285085
    reference: chr 8
allele count: 25
allele frequency: 2.037489812550937e-3
allele num: 12270
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+81G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+81G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+81G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.289G>A
  hgvsp: ENSP00000377318.3:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+81G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 16612
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 12999
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15562
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.75e1
  variant carriers: 12
hgvs: p.Ala97Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-12285086-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285086
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285086
    reference: chr 8
allele count: 267
allele frequency: 2.198978751441278e-2
allele num: 12142
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+80C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+80C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+80C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.288C>T
  hgvsp: ENST00000393715.3:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+80C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15796
  bin: 2.5e0
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 1.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15767
  bin: 7.5e0
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 9.75e1
  variant carriers: 242
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 6.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 2.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 13515
  bin: 2.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 3.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 6.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 14
hgvs: p.Gly96Gly
num of homozygotes: 8
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

8-12285088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285088
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285088
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 13224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+78G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+78G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.286G>A
  hgvsp: ENSP00000377318.3:p.Gly96Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+78G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+78G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15442
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14504
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14738
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly96Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

8-12285092-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285092
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285092
    reference: chr 8
allele count: 1
allele frequency: 7.164350193437455e-5
allele num: 13958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.282A>C
  hgvsp: ENSP00000377318.3:p.Glu94Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+74A>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+74A>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+74A>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+74A>C
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13845
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu94Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS

8-12285102-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285102
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285102
    reference: chr 8
allele count: 16847
allele frequency: 5.669717978057481e-1
allele num: 29714
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+64A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+64A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+64A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+64A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.272A>G
  hgvsp: ENSP00000377318.3:p.Glu91Gly
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 14315
  bin: 7.5e0
  variant carriers: 8364
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 253
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 557
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 1.75e1
  variant carriers: 3726
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 2.75e1
  variant carriers: 1064
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 2.25e1
  variant carriers: 2043
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 2.5e0
  variant carriers: 3067
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 1.25e1
  variant carriers: 5630
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 2.5e0
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 3603
  bin: 1.75e1
  variant carriers: 3050
genotype quality: GenotypeQuality
  all individuals: 6627
  bin: 2.25e1
  variant carriers: 2424
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 2.75e1
  variant carriers: 1007
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.75e1
  variant carriers: 415
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 9.25e1
  variant carriers: 191
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 10811
  bin: 9.75e1
  variant carriers: 10798
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.25e1
  variant carriers: 212
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 7.75e1
  variant carriers: 156
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 6.25e1
  variant carriers: 201
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.25e1
  variant carriers: 115
genotype quality: GenotypeQuality
  all individuals: 5603
  bin: 7.5e0
  variant carriers: 1402
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 1.25e1
  variant carriers: 1559
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.25e1
  variant carriers: 327
hgvs: p.Glu91Gly
num of homozygotes: 3401
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

8-12285103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285103
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285103
    reference: chr 8
allele count: 17054
allele frequency: 5.677097203728362e-1
allele num: 30040
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+63G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.271G>A
  hgvsp: ENSP00000377318.3:p.Glu91Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+63G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+63G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+63G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 2.25e1
  variant carriers: 2067
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7631
  bin: 2.5e0
  variant carriers: 2975
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 7.5e0
  variant carriers: 8322
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 1.25e1
  variant carriers: 5670
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 3.25e1
  variant carriers: 563
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 2.75e1
  variant carriers: 1082
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 1.75e1
  variant carriers: 3736
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 6.25e1
  variant carriers: 201
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 6.75e1
  variant carriers: 170
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.25e1
  variant carriers: 402
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 7.75e1
  variant carriers: 156
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.25e1
  variant carriers: 326
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 2.5e0
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 217
genotype quality: GenotypeQuality
  all individuals: 10810
  bin: 9.75e1
  variant carriers: 10797
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 1556
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.25e1
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 952
genotype quality: GenotypeQuality
  all individuals: 6706
  bin: 2.25e1
  variant carriers: 2426
genotype quality: GenotypeQuality
  all individuals: 5571
  bin: 7.5e0
  variant carriers: 1402
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 3.25e1
  variant carriers: 1339
hgvs: p.Glu91Lys
num of homozygotes: 3473
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/8-12285106-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285106
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285106
    reference: chr 8
allele count: 1
allele frequency: 3.227472243738704e-5
allele num: 30984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+60G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+60G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.268G>T
  hgvsp: ENSP00000377318.3:p.Val90Leu
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+60G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+60G>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9822
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3483
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8175
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val90Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

8-12285106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285106
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285106
    reference: chr 8
allele count: 9
allele frequency: 2.904725019364833e-4
allele num: 30984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+60G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+60G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.268G>A
  hgvsp: ENSP00000377318.3:p.Val90Met
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+60G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+60G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14427
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8175
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2492
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val90Met
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-12285110-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285110
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285110
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 31274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+56T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+56T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+56T>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.264T>C
  hgvsp: ENST00000393715.3:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+56T>C
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8120
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2955
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr88Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-12285128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285128
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285128
    reference: chr 8
allele count: 2
allele frequency: 4.018323555412682e-5
allele num: 49772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+38G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.246G>A
  hgvsp: ENST00000393715.3:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+38G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+38G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+38G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12675
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3995
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro82Pro
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-12285129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285129
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285129
    reference: chr 8
allele count: 4
allele frequency: 7.494847292486416e-5
allele num: 53370
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+37C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.245C>T
  hgvsp: ENSP00000377318.3:p.Pro82Leu
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+37C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+37C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+37C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19415
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3909
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro82Leu
num of homozygotes: 2
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

8-12285131-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285131
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285131
    reference: chr 8
allele count: 1
allele frequency: 1.742949768187681e-5
allele num: 57374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+35C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+35C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.243C>A
  hgvsp: ENSP00000377318.3:p.Cys81Ter
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+35C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+35C>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3828
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18656
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4567
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys81Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-12285132-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285132
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285132
    reference: chr 8
allele count: 17496
allele frequency: 2.836116064191928e-1
allele num: 61690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+34G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+34G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+34G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+34G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.242G>C
  hgvsp: ENSP00000377318.3:p.Cys81Ser
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 911
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 1132
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 7.5e0
  variant carriers: 1046
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.75e1
  variant carriers: 1097
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.75e1
  variant carriers: 1348
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 776
genotype depth: GenotypeDepth
  all individuals: 14219
  bin: 2.25e1
  variant carriers: 1354
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 3.25e1
  variant carriers: 1214
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.25e1
  variant carriers: 400
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 660
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 2.5e0
  variant carriers: 565
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 2.75e1
  variant carriers: 1297
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 856
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.25e1
  variant carriers: 1080
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 479
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.75e1
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 582
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 8.75e1
  variant carriers: 142
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 6.75e1
  variant carriers: 342
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 1.25e1
  variant carriers: 427
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 4.75e1
  variant carriers: 434
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 1.75e1
  variant carriers: 509
genotype quality: GenotypeQuality
  all individuals: 10043
  bin: 9.75e1
  variant carriers: 9683
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 3.25e1
  variant carriers: 408
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 2.75e1
  variant carriers: 295
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.25e1
  variant carriers: 291
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.25e1
  variant carriers: 200
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 3.75e1
  variant carriers: 483
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 7.75e1
  variant carriers: 244
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 2.5e0
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 7.5e0
  variant carriers: 425
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 5.25e1
  variant carriers: 446
hgvs: p.Cys81Ser
num of homozygotes: 3654
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-12285134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285134
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285134
    reference: chr 8
allele count: 3
allele frequency: 4.445234708392603e-5
allele num: 67488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.240G>A
  hgvsp: ENSP00000377318.3:p.Trp80Ter
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+32G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+32G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+32G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+32G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14330
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3614
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2977
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5016
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Trp80Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-12285135-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285135
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285135
    reference: chr 8
allele count: 3
allele frequency: 4.386477950637502e-5
allele num: 68392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+31G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.239G>T
  hgvsp: ENSP00000377318.3:p.Trp80Leu
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+31G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+31G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+31G>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15022
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Trp80Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-12285136-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285136
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285136
    reference: chr 8
allele count: 1
allele frequency: 1.44275161588181e-5
allele num: 69312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+30T>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+30T>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+30T>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+30T>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.238T>A
  hgvsp: ENSP00000377318.3:p.Trp80Arg
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15682
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Trp80Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP

8-12285139-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285139
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285139
    reference: chr 8
allele count: 3
allele frequency: 4.205332361434298e-5
allele num: 71338
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+27A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+27A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.235A>G
  hgvsp: ENSP00000377318.3:p.Thr79Ala
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+27A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+27A>G
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8856
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.75e1
  variant carriers: 1
hgvs: p.Thr79Ala
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

8-12285142-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285142
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285141
    reference: chr 8
allele count: 6
allele frequency: 8.348639171814995e-5
allele num: 71868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+23delG
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+23delG
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+23delG
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.231delG
  hgvsp: ENSP00000377318.3:p.Pro78LeufsTer15
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+23delG
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3068
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro78LeufsTer15
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: GC
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-12285143-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285143
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285143
    reference: chr 8
allele count: 2
allele frequency: 2.776697950796912e-5
allele num: 72028
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+23G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+23G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.231G>T
  hgvsp: ENST00000393715.3:c.231G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+23G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+23G>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3790
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3953
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly77Gly
num of homozygotes: 1
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS

8-12285145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285145
    reference: chr 8
allele count: 3
allele frequency: 4.107450915961554e-5
allele num: 73038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.229G>A
  hgvsp: ENSP00000377318.3:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+21G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+21G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+21G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+21G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly77Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-12285145-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285144
    reference: chr 8
allele count: 934
allele frequency: 1.278786385169364e-2
allele num: 73038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+20delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.228delC
  hgvsp: ENSP00000377318.3:p.Pro78LeufsTer15
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+20delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+20delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+20delC
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 19251
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 9.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 3.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 9.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 7.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 8.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 3.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 3.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 9320
  bin: 9.75e1
  variant carriers: 521
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 19
hgvs: p.Pro78LeufsTer15
num of homozygotes: 230
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: CG
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

8-12285146-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285146
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285146
    reference: chr 8
allele count: 3
allele frequency: 4.146166178340428e-5
allele num: 72356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.228C>A
  hgvsp: ENST00000393715.3:c.228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+20C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+20C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+20C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+20C>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18156
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8809
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro76Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

8-12285151-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285151
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285151
    reference: chr 8
allele count: 1
allele frequency: 1.338795619460733e-5
allele num: 74694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+15C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+15C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+15C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+15C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.223C>A
  hgvsp: ENSP00000377318.3:p.Pro75Thr
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4213
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18678
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro75Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-12285152-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285152
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285151
    reference: chr 8
allele count: 125
allele frequency: 1.66920385652859e-3
allele num: 74886
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+13delG
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.221delG
  hgvsp: ENSP00000377318.3:p.Arg74ProfsTer19
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+13delG
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+13delG
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+13delG
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20103
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4222
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9243
  bin: 9.75e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 3032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 18687
  bin: 6.25e1
  variant carriers: 2
hgvs: p.Arg74ProfsTer19
num of homozygotes: 36
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: GC
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

8-12285153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285153
    reference: chr 8
allele count: 4
allele frequency: 5.347450602925056e-5
allele num: 74802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+13G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.221G>A
  hgvsp: ENSP00000377318.3:p.Arg74His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+13G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+13G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+13G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20110
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4222
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg74His
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

8-12285154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285154
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285154
    reference: chr 8
allele count: 3
allele frequency: 4.000533404453927e-5
allele num: 74990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+12C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+12C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+12C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.220C>T
  hgvsp: ENSP00000377318.3:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+12C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9188
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18853
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg74Cys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

8-12285155-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285155
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285154
    reference: chr 8
allele count: 1
allele frequency: 1.328479953237506e-5
allele num: 75274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+10delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+10delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+10delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.218delC
  hgvsp: ENSP00000377318.3:p.Pro73HisfsTer20
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+10delC
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9247
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro73HisfsTer20
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: TG
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

8-12285157-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285157
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285157
    reference: chr 8
allele count: 2
allele frequency: 2.648375221801425e-5
allele num: 75518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.217C>A
  hgvsp: ENSP00000377318.3:p.Pro73Thr
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+9C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+9C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+9C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+9C>A
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4256
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2847
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro73Thr
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS

8-12285160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285160
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285160
    reference: chr 8
allele count: 13
allele frequency: 1.717486656449823e-4
allele num: 75692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+6C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.214C>T
  hgvsp: ENSP00000377318.3:p.Pro72Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+6C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+6C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+6C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3502
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9261
  bin: 9.75e1
  variant carriers: 7
hgvs: p.Pro72Ser
num of homozygotes: 5
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-12285161-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285161
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285161
    reference: chr 8
allele count: 54026
allele frequency: 6.83181588265048e-1
allele num: 79080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+5A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+5A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.213A>G
  hgvsp: ENST00000393715.3:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+5A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+5A>G
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 4.25e1
  variant carriers: 1918
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 1518
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 9.75e1
  variant carriers: 7688
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 3.25e1
  variant carriers: 2188
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.75e1
  variant carriers: 2203
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.25e1
  variant carriers: 1164
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.5e0
  variant carriers: 730
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 7.25e1
  variant carriers: 1182
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 9.25e1
  variant carriers: 866
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.25e1
  variant carriers: 1385
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 7.75e1
  variant carriers: 1181
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 4.75e1
  variant carriers: 1828
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 6.75e1
  variant carriers: 1319
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 8.25e1
  variant carriers: 1029
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 1.75e1
  variant carriers: 1393
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 8.75e1
  variant carriers: 1016
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 2036
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 2.25e1
  variant carriers: 1828
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 7.5e0
  variant carriers: 1129
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 1590
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 1.25e1
  variant carriers: 354
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 2.5e0
  variant carriers: 82
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.25e1
  variant carriers: 445
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 8.25e1
  variant carriers: 841
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.75e1
  variant carriers: 521
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 1.75e1
  variant carriers: 496
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.75e1
  variant carriers: 273
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 4.25e1
  variant carriers: 339
genotype quality: GenotypeQuality
  all individuals: 25745
  bin: 9.75e1
  variant carriers: 25484
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 4.75e1
  variant carriers: 500
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 5.75e1
  variant carriers: 403
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.75e1
  variant carriers: 446
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 7.75e1
  variant carriers: 813
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 7.5e0
  variant carriers: 490
hgvs: c.892+5A>G
num of homozygotes: 20932
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-12285165-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285165
    reference: chr 8
allele count: 6
allele frequency: 7.567158531971244e-5
allele num: 79290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.209G>C
  hgvsp: ENSP00000377318.3:p.Gly70Ala
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.790+1G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.790+1G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.892+1G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*62+1G>C
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6200
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
hgvs: c.892+1G>C
num of homozygotes: 2
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-12285172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285172
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285172
    reference: chr 8
allele count: 5
allele frequency: 6.304057291272662e-5
allele num: 79314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*56G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.886G>A
  hgvsp: ENSP00000262365.4:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.784G>A
  hgvsp: ENSP00000432491.1:p.Glu262Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.202G>A
  hgvsp: ENSP00000377318.3:p.Glu68Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.784G>A
  hgvsp: ENSP00000283479.4:p.Glu262Lys
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23842
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4130
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu296Lys
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ

8-12285173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285173
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285173
    reference: chr 8
allele count: 23
allele frequency: 2.895266868076536e-4
allele num: 79440
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.885C>T
  hgvsp: ENST00000262365.4:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*55C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.783C>T
  hgvsp: ENST00000351291.4:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.783C>T
  hgvsp: ENST00000527331.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.201C>T
  hgvsp: ENST00000393715.3:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3646
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6266
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24052
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr295Thr
num of homozygotes: 7
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-12285174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285174
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285174
    reference: chr 8
allele count: 1
allele frequency: 1.258494840171155e-5
allele num: 79460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.200C>T
  hgvsp: ENSP00000377318.3:p.Thr67Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.884C>T
  hgvsp: ENSP00000262365.4:p.Thr295Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.782C>T
  hgvsp: ENSP00000432491.1:p.Thr261Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*54C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.782C>T
  hgvsp: ENSP00000283479.4:p.Thr261Ile
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3719
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr295Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

8-12285176-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285176
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285176
    reference: chr 8
allele count: 2
allele frequency: 2.51559669953713e-5
allele num: 79504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*52C>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.780C>G
  hgvsp: ENST00000351291.4:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.198C>G
  hgvsp: ENST00000393715.3:c.198C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.882C>G
  hgvsp: ENST00000262365.4:c.882C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.780C>G
  hgvsp: ENST00000527331.1:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3795
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1268
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4132
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr294Thr
num of homozygotes: 1
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-12285177-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285177
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285177
    reference: chr 8
allele count: 1
allele frequency: 1.257735070684711e-5
allele num: 79508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.197C>T
  hgvsp: ENSP00000377318.3:p.Thr66Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*51C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.881C>T
  hgvsp: ENSP00000262365.4:p.Thr294Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.779C>T
  hgvsp: ENSP00000432491.1:p.Thr260Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.779C>T
  hgvsp: ENSP00000283479.4:p.Thr260Ile
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3803
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr294Ile
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

8-12285177-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285177
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285177
    reference: chr 8
allele count: 8
allele frequency: 1.006188056547769e-4
allele num: 79508
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.881C>G
  hgvsp: ENSP00000262365.4:p.Thr294Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.779C>G
  hgvsp: ENSP00000283479.4:p.Thr260Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.197C>G
  hgvsp: ENSP00000377318.3:p.Thr66Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*51C>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.779C>G
  hgvsp: ENSP00000432491.1:p.Thr260Ser
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3803
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr294Ser
num of homozygotes: 2
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-12285179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285179
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285179
    reference: chr 8
allele count: 8
allele frequency: 1.006086825293023e-4
allele num: 79516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.777C>T
  hgvsp: ENST00000527331.1:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.195C>T
  hgvsp: ENST00000393715.3:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.879C>T
  hgvsp: ENST00000262365.4:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*49C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.777C>T
  hgvsp: ENST00000351291.4:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24608
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe293Phe
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

8-12285184-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285184
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285184
    reference: chr 8
allele count: 10
allele frequency: 1.255997387525434e-4
allele num: 79618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.772C>G
  hgvsp: ENSP00000283479.4:p.Leu258Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.874C>G
  hgvsp: ENSP00000262365.4:p.Leu292Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.190C>G
  hgvsp: ENSP00000377318.3:p.Leu64Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*44C>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.772C>G
  hgvsp: ENSP00000432491.1:p.Leu258Val
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4104
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu292Val
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-12285186-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285186
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285186
    reference: chr 8
allele count: 1
allele frequency: 1.255366692610912e-5
allele num: 79658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.770A>C
  hgvsp: ENSP00000432491.1:p.Gln257Pro
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.188A>C
  hgvsp: ENSP00000377318.3:p.Gln63Pro
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.872A>C
  hgvsp: ENSP00000262365.4:p.Gln291Pro
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.770A>C
  hgvsp: ENSP00000283479.4:p.Gln257Pro
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*42A>C
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24878
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3916
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln291Pro
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-12285188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285188
    reference: chr 8
allele count: 1
allele frequency: 1.255555834567963e-5
allele num: 79646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.186C>T
  hgvsp: ENST00000393715.3:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*40C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.768C>T
  hgvsp: ENST00000527331.1:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.768C>T
  hgvsp: ENST00000351291.4:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.870C>T
  hgvsp: ENST00000262365.4:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24816
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys290Cys
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-12285189-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285189
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285189
    reference: chr 8
allele count: 2
allele frequency: 2.510544286001205e-5
allele num: 79664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.767G>T
  hgvsp: ENSP00000432491.1:p.Cys256Phe
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*39G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.767G>T
  hgvsp: ENSP00000283479.4:p.Cys256Phe
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.185G>T
  hgvsp: ENSP00000377318.3:p.Cys62Phe
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.869G>T
  hgvsp: ENSP00000262365.4:p.Cys290Phe
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys290Phe
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

8-12285196-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285196
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285196
    reference: chr 8
allele count: 1
allele frequency: 1.259223814440779e-5
allele num: 79414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*32G>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.178G>C
  hgvsp: ENSP00000377318.3:p.Glu60Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.862G>C
  hgvsp: ENSP00000262365.4:p.Glu288Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.760G>C
  hgvsp: ENSP00000283479.4:p.Glu254Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.760G>C
  hgvsp: ENSP00000432491.1:p.Glu254Gln
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6275
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu288Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

8-12285200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285200
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285200
    reference: chr 8
allele count: 1
allele frequency: 1.264318405947354e-5
allele num: 79094
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.858C>T
  hgvsp: ENST00000262365.4:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.174C>T
  hgvsp: ENST00000393715.3:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.756C>T
  hgvsp: ENST00000351291.4:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*28C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.756C>T
  hgvsp: ENST00000527331.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6043
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn286Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

8-12285201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285201
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285201
    reference: chr 8
allele count: 3
allele frequency: 3.79285931020532e-5
allele num: 79096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*27A>G
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.173A>G
  hgvsp: ENSP00000377318.3:p.Asn58Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.755A>G
  hgvsp: ENSP00000283479.4:p.Asn252Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.857A>G
  hgvsp: ENSP00000262365.4:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.755A>G
  hgvsp: ENSP00000432491.1:p.Asn252Ser
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4093
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 23376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6047
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn286Ser
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-12285202-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285202
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285202
    reference: chr 8
allele count: 5116
allele frequency: 6.461390790371063e-2
allele num: 79178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.172A>C
  hgvsp: ENSP00000377318.3:p.Asn58His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*26A>C
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.856A>C
  hgvsp: ENSP00000262365.4:p.Asn286His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.754A>C
  hgvsp: ENSP00000283479.4:p.Asn252His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.754A>C
  hgvsp: ENSP00000432491.1:p.Asn252His
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.75e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 2.75e1
  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 3.25e1
  variant carriers: 225
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 4.25e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 994
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 7.5e0
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.75e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 2.25e1
  variant carriers: 267
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.25e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 2.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.75e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.5e0
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 73
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.25e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 7.5e0
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 5992
  bin: 6.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.25e1
  variant carriers: 74
genotype quality: GenotypeQuality
  all individuals: 23040
  bin: 6.25e1
  variant carriers: 86
hgvs: p.Asn286His
num of homozygotes: 1384
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

8-12285203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285203
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285203
    reference: chr 8
allele count: 3
allele frequency: 3.796699402652627e-5
allele num: 79016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.171C>T
  hgvsp: ENST00000393715.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.753C>T
  hgvsp: ENST00000527331.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*25C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.753C>T
  hgvsp: ENST00000351291.4:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.855C>T
  hgvsp: ENST00000262365.4:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg285Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

8-12285204-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285204
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285204
    reference: chr 8
allele count: 38
allele frequency: 4.813294826974717e-4
allele num: 78948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.752G>A
  hgvsp: ENSP00000283479.4:p.Arg251His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.752G>A
  hgvsp: ENSP00000432491.1:p.Arg251His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*24G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.854G>A
  hgvsp: ENSP00000262365.4:p.Arg285His
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.170G>A
  hgvsp: ENSP00000377318.3:p.Arg57His
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 9.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Arg285His
num of homozygotes: 6
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-12285204-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285204
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285203
    reference: chr 8
allele count: 1
allele frequency: 1.266656533414399e-5
allele num: 78948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.751delC
  hgvsp: ENSP00000283479.4:p.Arg251AlafsTer13
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*23delC
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.751delC
  hgvsp: ENSP00000432491.1:p.Arg251AlafsTer13
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.853delC
  hgvsp: ENSP00000262365.4:p.Arg285AlafsTer13
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.169delC
  hgvsp: ENSP00000377318.3:p.Arg57AlafsTer13
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg285AlafsTer13
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: CG
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

8-12285205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285205
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285205
    reference: chr 8
allele count: 470
allele frequency: 5.966890107657932e-3
allele num: 78768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.751C>T
  hgvsp: ENSP00000432491.1:p.Arg251Cys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.169C>T
  hgvsp: ENSP00000377318.3:p.Arg57Cys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.751C>T
  hgvsp: ENSP00000283479.4:p.Arg251Cys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*23C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.853C>T
  hgvsp: ENSP00000262365.4:p.Arg285Cys
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 2.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 3594
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 295
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6318
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 24093
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 2
hgvs: p.Arg285Cys
num of homozygotes: 127
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-12285205-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285205
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285205
    reference: chr 8
allele count: 131
allele frequency: 1.663111923623807e-3
allele num: 78768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.169C>A
  hgvsp: ENSP00000377318.3:p.Arg57Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.751C>A
  hgvsp: ENSP00000283479.4:p.Arg251Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.853C>A
  hgvsp: ENSP00000262365.4:p.Arg285Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*23C>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.751C>A
  hgvsp: ENSP00000432491.1:p.Arg251Ser
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3594
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 24093
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 1
hgvs: p.Arg285Ser
num of homozygotes: 21
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-12285208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285208
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285208
    reference: chr 8
allele count: 3
allele frequency: 3.812525416836112e-5
allele num: 78688
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.850G>A
  hgvsp: ENSP00000262365.4:p.Val284Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.166G>A
  hgvsp: ENSP00000377318.3:p.Val56Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.748G>A
  hgvsp: ENSP00000283479.4:p.Val250Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.748G>A
  hgvsp: ENSP00000432491.1:p.Val250Ile
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*20G>A
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24302
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val284Ile
num of homozygotes: 1
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

8-12285209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285209
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285209
    reference: chr 8
allele count: 1
allele frequency: 1.271100264388855e-5
allele num: 78672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.747C>T
  hgvsp: ENST00000351291.4:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.747C>T
  hgvsp: ENST00000527331.1:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.165C>T
  hgvsp: ENST00000393715.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.849C>T
  hgvsp: ENST00000262365.4:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*19C>T
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7572
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr283Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

8-12285220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285220
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285220
    reference: chr 8
allele count: 5
allele frequency: 6.417826153925142e-5
allele num: 77908
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.838G>A
  hgvsp: ENSP00000262365.4:p.Val280Met
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*8G>A
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.154G>A
  hgvsp: ENSP00000377318.3:p.Val52Met
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.736G>A
  hgvsp: ENSP00000283479.4:p.Val246Met
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.736G>A
  hgvsp: ENSP00000432491.1:p.Val246Met
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6098
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val280Met
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-12285220-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285220
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285220
    reference: chr 8
allele count: 1
allele frequency: 1.283565230785028e-5
allele num: 77908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.154G>T
  hgvsp: ENSP00000377318.3:p.Val52Leu
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*8G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.838G>T
  hgvsp: ENSP00000262365.4:p.Val280Leu
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.736G>T
  hgvsp: ENSP00000432491.1:p.Val246Leu
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.736G>T
  hgvsp: ENSP00000283479.4:p.Val246Leu
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6098
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val280Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-12285221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285221
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285221
    reference: chr 8
allele count: 8
allele frequency: 1.027907693889089e-4
allele num: 77828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.735C>T
  hgvsp: ENST00000351291.4:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*7C>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.735C>T
  hgvsp: ENST00000527331.1:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.837C>T
  hgvsp: ENST00000262365.4:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.153C>T
  hgvsp: ENST00000393715.3:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr279Tyr
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/8-12285227-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285227
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285227
    reference: chr 8
allele count: 1
allele frequency: 1.291756013124241e-5
allele num: 77414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.729G>T
  hgvsp: ENSP00000432491.1:p.Glu243Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.*1G>T
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.729G>T
  hgvsp: ENSP00000283479.4:p.Glu243Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.147G>T
  hgvsp: ENSP00000377318.3:p.Glu49Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.831G>T
  hgvsp: ENSP00000262365.4:p.Glu277Asp
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu277Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

8-12285229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285229
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285229
    reference: chr 8
allele count: 2
allele frequency: 2.587991718426501e-5
allele num: 77280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.727G>A
  hgvsp: ENSP00000283479.4:p.Glu243Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.829G>A
  hgvsp: ENSP00000262365.4:p.Glu277Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.727G>A
  hgvsp: ENSP00000432491.1:p.Glu243Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.145G>A
  hgvsp: ENSP00000377318.3:p.Glu49Lys
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.461G>A
  hgvsp: ENST00000309608.5:c.461G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20329
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu277Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

8-12285232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285232
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285232
    reference: chr 8
allele count: 195
allele frequency: 2.536420395421436e-3
allele num: 76880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.724C>T
  hgvsp: ENSP00000432491.1:p.Pro242Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.142C>T
  hgvsp: ENSP00000377318.3:p.Pro48Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.724C>T
  hgvsp: ENSP00000283479.4:p.Pro242Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.826C>T
  hgvsp: ENSP00000262365.4:p.Pro276Ser
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.458C>T
  hgvsp: ENSP00000311330.5:p.Ser153Phe
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 5498
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9155
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18913
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 9.75e1
  variant carriers: 108
hgvs: p.Pro276Ser
num of homozygotes: 52
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-12285234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285234
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285234
    reference: chr 8
allele count: 3
allele frequency: 3.945188185476447e-5
allele num: 76042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.722C>T
  hgvsp: ENSP00000283479.4:p.Ala241Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.140C>T
  hgvsp: ENSP00000377318.3:p.Ala47Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.456C>T
  hgvsp: ENST00000309608.5:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.824C>T
  hgvsp: ENSP00000262365.4:p.Ala275Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.722C>T
  hgvsp: ENSP00000432491.1:p.Ala241Val
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala275Val
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

8-12285234-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285234
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285234
    reference: chr 8
allele count: 1
allele frequency: 1.315062728492149e-5
allele num: 76042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.722C>A
  hgvsp: ENSP00000283479.4:p.Ala241Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.140C>A
  hgvsp: ENSP00000377318.3:p.Ala47Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.456C>A
  hgvsp: ENST00000309608.5:c.456C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.824C>A
  hgvsp: ENSP00000262365.4:p.Ala275Asp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.722C>A
  hgvsp: ENSP00000432491.1:p.Ala241Asp
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala275Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

8-12285237-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285237
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285237
    reference: chr 8
allele count: 3
allele frequency: 3.98215992354253e-5
allele num: 75336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.719G>A
  hgvsp: ENSP00000283479.4:p.Arg240Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.453G>A
  hgvsp: ENST00000309608.5:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.719G>A
  hgvsp: ENSP00000432491.1:p.Arg240Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.821G>A
  hgvsp: ENSP00000262365.4:p.Arg274Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.137G>A
  hgvsp: ENSP00000377318.3:p.Arg46Gln
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3075
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11580
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg274Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

8-12285238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285238
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285238
    reference: chr 8
allele count: 11
allele frequency: 1.460513038398216e-4
allele num: 75316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.718C>T
  hgvsp: ENSP00000432491.1:p.Arg240Trp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.136C>T
  hgvsp: ENSP00000377318.3:p.Arg46Trp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.452C>T
  hgvsp: ENSP00000311330.5:p.Ala151Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.820C>T
  hgvsp: ENSP00000262365.4:p.Arg274Trp
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.718C>T
  hgvsp: ENSP00000283479.4:p.Arg240Trp
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 11691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4713
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg274Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

8-12285241-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285241
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285241
    reference: chr 8
allele count: 29
allele frequency: 4.024870926553045e-4
allele num: 72052
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.817A>C
  hgvsp: ENSP00000262365.4:p.Lys273Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.133A>C
  hgvsp: ENSP00000377318.3:p.Lys45Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.449A>C
  hgvsp: ENSP00000311330.5:p.Gln150Pro
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.715A>C
  hgvsp: ENSP00000283479.4:p.Lys239Gln
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.715A>C
  hgvsp: ENSP00000432491.1:p.Lys239Gln
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13718
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3852
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 3.75e1
  variant carriers: 1
hgvs: p.Lys273Gln
num of homozygotes: 4
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

8-12285242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285242
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285242
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 70926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.714C>T
  hgvsp: ENST00000527331.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.714C>T
  hgvsp: ENST00000351291.4:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.816C>T
  hgvsp: ENST00000262365.4:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.448C>T
  hgvsp: ENSP00000311330.5:p.Gln150Ter
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.132C>T
  hgvsp: ENST00000393715.3:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/32222
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4080
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12784
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3669
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln150Ter
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-12285244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285244
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285244
    reference: chr 8
allele count: 3
allele frequency: 4.542426261280358e-5
allele num: 66044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.446C>T
  hgvsp: ENSP00000311330.5:p.Ala149Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000436338
  ensembl transcript: ENST00000532480
  gene symbol: FAM86B2
  hgvsc: ENST00000532480.1:c.446C>T
  hgvsp: ENSP00000436338.1:p.Ala149Val
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.712C>T
  hgvsp: ENSP00000432491.1:p.His238Tyr
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.814C>T
  hgvsp: ENSP00000262365.4:p.His272Tyr
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.130C>T
  hgvsp: ENSP00000377318.3:p.His44Tyr
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.712C>T
  hgvsp: ENSP00000283479.4:p.His238Tyr
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His272Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

8-12285246-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12285246
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 12285245
    reference: chr 8
allele count: 1
allele frequency: 1.560792882784454e-5
allele num: 64070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000436338
  ensembl transcript: ENST00000532480
  gene symbol: FAM86B2
  hgvsc: ENST00000532480.1:c.443delG
  hgvsp: ENSP00000436338.1:p.Gly148GlufsTer?
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000432491
  ensembl transcript: ENST00000527331
  gene symbol: FAM86B2
  hgvsc: ENST00000527331.1:c.709delG
  hgvsp: ENSP00000432491.1:p.Glu237SerfsTer27
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000377318
  ensembl transcript: ENST00000393715
  gene symbol: FAM86B2
  hgvsc: ENST00000393715.3:c.127delG
  hgvsp: ENSP00000377318.3:p.Glu43SerfsTer27
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000283479
  ensembl transcript: ENST00000351291
  gene symbol: FAM86B2
  hgvsc: ENST00000351291.4:c.709delG
  hgvsp: ENSP00000283479.4:p.Glu237SerfsTer27
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000311330
  ensembl transcript: ENST00000309608
  gene symbol: FAM86B2
  hgvsc: ENST00000309608.5:c.443delG
  hgvsp: ENSP00000311330.5:p.Gly148GlufsTer61
  variant of: http://identifiers.org/hgnc/32222
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145002
  ensembl protein: ENSP00000262365
  ensembl transcript: ENST00000262365
  gene symbol: FAM86B2
  hgvsc: ENST00000262365.4:c.811delG
  hgvsp: ENSP00000262365.4:p.Glu271SerfsTer27
  variant of: http://identifiers.org/hgnc/32222
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14750
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5478
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9294
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu271SerfsTer27
num of homozygotes: 0
reference allele: TC

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

GenotypeQuality
all individuals: 454
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 938
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.537735849056604e-3
allele num: 848
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQ
type: SiteQuality
SIO_000300: 2.183e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.05e-1

DP
type: SiteQuality
SIO_000300: 1.31648e5

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.64e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.529e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

GenotypeQuality
all individuals: 9
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.782e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 1.48188e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 2.176e1

QD
type: SiteQuality
SIO_000300: 6.79e0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.629629629629629e-3
allele num: 216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1312
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -6.011e0

QD
type: SiteQuality
SIO_000300: 3.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 2.2e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.68e-2

DP
type: SiteQuality
SIO_000300: 1.64496e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 547
bin: 3.75e1
variant carriers: 491

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 133

GenotypeQuality
all individuals: 570
bin: 6.25e1
variant carriers: 301

GenotypeQuality
all individuals: 1787
bin: 9.75e1
variant carriers: 1783

GenotypeQuality
all individuals: 250
bin: 4.75e1
variant carriers: 225

East Asian
type: Population
allele count: 337
allele frequency: 4.706703910614525e-1
allele num: 716
num of homozygotes: 15

African
type: Population
allele count: 57
allele frequency: 2.050359712230216e-1
allele num: 278
num of homozygotes: 2

South Asian
type: Population
allele count: 650
allele frequency: 3.312945973496432e-1
allele num: 1962
num of homozygotes: 37

Latino
type: Population
allele count: 249
allele frequency: 4.825581395348837e-1
allele num: 516
num of homozygotes: 21

European (Finnish)
type: Population
allele count: 157
allele frequency: 5.48951048951049e-1
allele num: 286
num of homozygotes: 17

Other
type: Population
allele count: 36
allele frequency: 4.615384615384616e-1
allele num: 78
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 2571
allele frequency: 4.923400995787055e-1
allele num: 5222
num of homozygotes: 160

DP
type: SiteQuality
SIO_000300: 2.02922e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.354e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 2.182e1

GenotypeQuality
all individuals: 1375
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10556
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 4.266211604095563e-4
allele num: 2344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 1.470588235294118e-2
allele num: 340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.25e-2

DP
type: SiteQuality
SIO_000300: 2.22139e5

FS
type: SiteQuality
SIO_000300: 2.119e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.082e0

MQ
type: SiteQuality
SIO_000300: 2.2e1

QD
type: SiteQuality
SIO_000300: 4.88e0

GenotypeQuality
all individuals: 84
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 817
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 2.368421052631579e-2
allele num: 380
num of homozygotes: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6012
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.474926253687316e-3
allele num: 678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.051e1

FS
type: SiteQuality
SIO_000300: 3.88e0

MQ
type: SiteQuality
SIO_000300: 2.2e1

DP
type: SiteQuality
SIO_000300: 2.26112e5

VQSLOD
type: SiteQuality
SIO_000300: -6.462e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.71e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
all individuals: 96
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 13

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 295
bin: 9.75e1
variant carriers: 210

East Asian
type: Population
allele count: 3
allele frequency: 3.006012024048096e-3
allele num: 998
num of homozygotes: 0

African
type: Population
allele count: 71
allele frequency: 1.606334841628959e-1
allele num: 442
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 9.234828496042216e-3
allele num: 758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 5.3475935828877e-3
allele num: 374
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 9.803921568627451e-3
allele num: 102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 58
allele frequency: 9.105180533751962e-3
allele num: 6370
num of homozygotes: 0

South Asian
type: Population
allele count: 35
allele frequency: 1.384493670886076e-2
allele num: 2528
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.193e1

DP
type: SiteQuality
SIO_000300: 2.46864e5

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 7.168e0

QD
type: SiteQuality
SIO_000300: 1.212e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.272e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

GenotypeQuality
all individuals: 1406
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 67
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 12
allele frequency: 1.142857142857143e-2
allele num: 1050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 8.620689655172414e-3
allele num: 580
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 2.242152466367713e-3
allele num: 2676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-4
allele num: 6664
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.240694789081886e-3
allele num: 806
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.456e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.181e0

DP
type: SiteQuality
SIO_000300: 2.52471e5

QD
type: SiteQuality
SIO_000300: 7.06e0

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 2.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 1347
bin: 2.5e0
variant carriers: 24

GenotypeQuality
all individuals: 990
bin: 1.75e1
variant carriers: 70

GenotypeQuality
all individuals: 14807
bin: 7.5e0
variant carriers: 138

GenotypeQuality
all individuals: 1345
bin: 3.25e1
variant carriers: 21

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 17

Latino
type: Population
allele count: 16
allele frequency: 1.951219512195122e-2
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 3.745318352059925e-3
allele num: 1068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 67
allele frequency: 1.015459230069718e-2
allele num: 6598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 5.208333333333333e-3
allele num: 384
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 1.923076923076923e-2
allele num: 104
num of homozygotes: 0

African
type: Population
allele count: 140
allele frequency: 2.592592592592592e-1
allele num: 540
num of homozygotes: 8

South Asian
type: Population
allele count: 36
allele frequency: 1.36986301369863e-2
allele num: 2628
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.183e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.81e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 4.865e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

VQSLOD
type: SiteQuality
SIO_000300: -4.709e0

QD
type: SiteQuality
SIO_000300: 1.195e1

DP
type: SiteQuality
SIO_000300: 2.60755e5

GenotypeQuality
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7136
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1138
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.791e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.418e0

DP
type: SiteQuality
SIO_000300: 2.69549e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-2

MQ
type: SiteQuality
SIO_000300: 2.2e1

GenotypeQuality
all individuals: 1104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.330140994945464e-4
allele num: 7518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1226
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2934
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.08e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.296e0

DP
type: SiteQuality
SIO_000300: 2.81999e5

MQ
type: SiteQuality
SIO_000300: 2.185e1

QD
type: SiteQuality
SIO_000300: 2.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 207
bin: 6.75e1
variant carriers: 171

GenotypeQuality
all individuals: 432
bin: 4.25e1
variant carriers: 402

GenotypeQuality
all individuals: 1616
bin: 3.25e1
variant carriers: 1340

GenotypeQuality
all individuals: 1084
bin: 3.75e1
variant carriers: 950

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 216

East Asian
type: Population
allele count: 1755
allele frequency: 5.675937904269082e-1
allele num: 3092
num of homozygotes: 271

South Asian
type: Population
allele count: 3145
allele frequency: 5.837045285820341e-1
allele num: 5388
num of homozygotes: 690

African
type: Population
allele count: 546
allele frequency: 5.150943396226415e-1
allele num: 1060
num of homozygotes: 103

European (Non-Finnish)
type: Population
allele count: 8238
allele frequency: 5.304571796522859e-1
allele num: 15530
num of homozygotes: 1368

European (Finnish)
type: Population
allele count: 698
allele frequency: 5.749588138385503e-1
allele num: 1214
num of homozygotes: 146

Other
type: Population
allele count: 117
allele frequency: 5.679611650485437e-1
allele num: 206
num of homozygotes: 22

Latino
type: Population
allele count: 2348
allele frequency: 7.28287841191067e-1
allele num: 3224
num of homozygotes: 801

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

VQSLOD
type: SiteQuality
SIO_000300: 1.308e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.12693e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.576e1

MQ
type: SiteQuality
SIO_000300: 2.168e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.225e-1

GenotypeQuality
all individuals: 3560
bin: 1.75e1
variant carriers: 3050

GenotypeQuality
all individuals: 193
bin: 9.25e1
variant carriers: 191

GenotypeQuality
all individuals: 466
bin: 4.75e1
variant carriers: 415

GenotypeQuality
all individuals: 1289
bin: 2.75e1
variant carriers: 1008

GenotypeQuality
all individuals: 219
bin: 8.25e1
variant carriers: 212

South Asian
type: Population
allele count: 3169
allele frequency: 5.849021779254338e-1
allele num: 5418
num of homozygotes: 697

Latino
type: Population
allele count: 2384
allele frequency: 7.286063569682152e-1
allele num: 3272
num of homozygotes: 818

African
type: Population
allele count: 563
allele frequency: 5.184162062615101e-1
allele num: 1086
num of homozygotes: 110

Other
type: Population
allele count: 117
allele frequency: 5.679611650485437e-1
allele num: 206
num of homozygotes: 22

East Asian
type: Population
allele count: 1772
allele frequency: 5.68313021167415e-1
allele num: 3118
num of homozygotes: 277

European (Finnish)
type: Population
allele count: 710
allele frequency: 5.772357723577236e-1
allele num: 1230
num of homozygotes: 150

European (Non-Finnish)
type: Population
allele count: 8339
allele frequency: 5.30808402291534e-1
allele num: 15710
num of homozygotes: 1399

DP
type: SiteQuality
SIO_000300: 4.17738e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-1

MQ
type: SiteQuality
SIO_000300: 2.168e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.312e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

QD
type: SiteQuality
SIO_000300: 2.52e1

VQSLOD
type: SiteQuality
SIO_000300: 1.313e1

GenotypeQuality
all individuals: 2492
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 8.169934640522876e-4
allele num: 1224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

VQSLOD
type: SiteQuality
SIO_000300: -6.29e0

MQ
type: SiteQuality
SIO_000300: 2.155e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.11758e5

QD
type: SiteQuality
SIO_000300: 5.88e0

GenotypeQuality
all individuals: 3483
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9822
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 3.25e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.965599051008304e-4
allele num: 3372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3240
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.492537313432836e-3
allele num: 5360
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

DP
type: SiteQuality
SIO_000300: 4.11758e5

MQ
type: SiteQuality
SIO_000300: 2.155e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 5.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

GenotypeQuality
all individuals: 266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3388
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.17508e5

MQRankSum
type: SiteQuality
SIO_000300: -1.064e0

MQ
type: SiteQuality
SIO_000300: 2.111e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: -7.383e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.79e-1

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.576331540268203e-5
allele num: 26398
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.432e0

FS
type: SiteQuality
SIO_000300: 5.268e0

MQ
type: SiteQuality
SIO_000300: 2.761e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.486e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 6.83124e5

QD
type: SiteQuality
SIO_000300: 1.483e1

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16992
bin: 6.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.063144511936714e-5
allele num: 28316
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 3.5486160397445e-4
allele num: 5636
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.567e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.038e0

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 3.455e1

DP
type: SiteQuality
SIO_000300: 7.16383e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

MQ
type: SiteQuality
SIO_000300: 2.585e1

GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2880
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.869158878504673e-4
allele num: 5350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30440
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.603e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

FS
type: SiteQuality
SIO_000300: 1.066e0

VQSLOD
type: SiteQuality
SIO_000300: -5.234e0

MQRankSum
type: SiteQuality
SIO_000300: -1.286e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

DP
type: SiteQuality
SIO_000300: 7.49286e5

QD
type: SiteQuality
SIO_000300: 6.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

GenotypeQuality
all individuals: 5984
bin: 2.25e1
variant carriers: 430

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 281

GenotypeQuality
all individuals: 505
bin: 8.25e1
variant carriers: 196

GenotypeQuality
all individuals: 361
bin: 9.25e1
variant carriers: 191

GenotypeQuality
all individuals: 11283
bin: 6.25e1
variant carriers: 367

South Asian
type: Population
allele count: 1402
allele frequency: 1.411314676867324e-1
allele num: 9934
num of homozygotes: 228

East Asian
type: Population
allele count: 1436
allele frequency: 2.591122338505955e-1
allele num: 5542
num of homozygotes: 202

Latino
type: Population
allele count: 1415
allele frequency: 2.195159789016444e-1
allele num: 6446
num of homozygotes: 326

African
type: Population
allele count: 1168
allele frequency: 3.758043758043758e-1
allele num: 3108
num of homozygotes: 260

European (Finnish)
type: Population
allele count: 1015
allele frequency: 3.272082527401676e-1
allele num: 3102
num of homozygotes: 264

European (Non-Finnish)
type: Population
allele count: 10946
allele frequency: 3.302558532464398e-1
allele num: 33144
num of homozygotes: 2348

Other
type: Population
allele count: 114
allele frequency: 2.753623188405797e-1
allele num: 414
num of homozygotes: 26

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

QD
type: SiteQuality
SIO_000300: 1.069e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

FS
type: SiteQuality
SIO_000300: 6.36e-1

DP
type: SiteQuality
SIO_000300: 1.136345e6

MQ
type: SiteQuality
SIO_000300: 2.815e1

VQSLOD
type: SiteQuality
SIO_000300: 2.384e1

MQRankSum
type: SiteQuality
SIO_000300: -4.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.745e-1

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8824
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6960
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.794336810730253e-4
allele num: 10736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35840
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.194839e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.879e0

MQ
type: SiteQuality
SIO_000300: 2.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

QD
type: SiteQuality
SIO_000300: 7.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

GenotypeQuality
all individuals: 781
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8834
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 7.302823758519961e-4
allele num: 4108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7050
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.135e0

DP
type: SiteQuality
SIO_000300: 1.204114e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

QD
type: SiteQuality
SIO_000300: 1.399e1

VQSLOD
type: SiteQuality
SIO_000300: -4.571e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

MQ
type: SiteQuality
SIO_000300: 2.831e1

GenotypeQuality
all individuals: 790
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8847
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3799
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.618122977346278e-4
allele num: 6180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7152
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.901e0

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

QD
type: SiteQuality
SIO_000300: 3.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQ
type: SiteQuality
SIO_000300: 3.245e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

FS
type: SiteQuality
SIO_000300: 3.213e0

DP
type: SiteQuality
SIO_000300: 1.213124e6

GenotypeQuality
all individuals: 830
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 815
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.309546564723373e-5
allele num: 37668
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.29147571035747e-4
allele num: 4364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.135e0

QD
type: SiteQuality
SIO_000300: 9.42e0

DP
type: SiteQuality
SIO_000300: 1.235714e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: -7.74e0

FS
type: SiteQuality
SIO_000300: 2.2745e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.42e-1

MQ
type: SiteQuality
SIO_000300: 2.596e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8876
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 829
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3942
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.750393838613688e-4
allele num: 11426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.054351837208076e-4
allele num: 37938
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.513e1

FS
type: SiteQuality
SIO_000300: 3.052e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

MQ
type: SiteQuality
SIO_000300: 2.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.243561e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

GenotypeQuality
all individuals: 670
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8879
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.747335313646689e-4
allele num: 11446
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3826
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.287e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.975e1

DP
type: SiteQuality
SIO_000300: 1.245763e6

VQSLOD
type: SiteQuality
SIO_000300: -6.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9320
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 2
allele frequency: 1.724137931034483e-4
allele num: 11600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.337255950788981e-4
allele num: 7478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

DP
type: SiteQuality
SIO_000300: 1.270251e6

MQ
type: SiteQuality
SIO_000300: 2.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.116e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 15

GenotypeQuality
all individuals: 871
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 17766
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 14

GenotypeQuality
all individuals: 3963
bin: 6.75e1
variant carriers: 14

African
type: Population
allele count: 118
allele frequency: 2.606007067137809e-2
allele num: 4528
num of homozygotes: 21

Latino
type: Population
allele count: 55
allele frequency: 7.354907729339395e-3
allele num: 7478
num of homozygotes: 8

East Asian
type: Population
allele count: 40
allele frequency: 6.195786864931847e-3
allele num: 6456
num of homozygotes: 8

South Asian
type: Population
allele count: 148
allele frequency: 1.275862068965517e-2
allele num: 11600
num of homozygotes: 42

European (Non-Finnish)
type: Population
allele count: 434
allele frequency: 1.12668743509865e-2
allele num: 38520
num of homozygotes: 117

European (Finnish)
type: Population
allele count: 131
allele frequency: 3.308080808080808e-2
allele num: 3960
num of homozygotes: 31

Other
type: Population
allele count: 8
allele frequency: 1.612903225806452e-2
allele num: 496
num of homozygotes: 3

QD
type: SiteQuality
SIO_000300: 1.345e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.116e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

DP
type: SiteQuality
SIO_000300: 1.270251e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 2.962e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 3306
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38226
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.554243083618278e-4
allele num: 6434
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.738223535546671e-4
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.238638e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.454e0

MQ
type: SiteQuality
SIO_000300: 2.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 8.032e0

VQSLOD
type: SiteQuality
SIO_000300: -4.691e0

QD
type: SiteQuality
SIO_000300: 8.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

GenotypeQuality
all individuals: 708
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3068
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4814
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.525785779676533e-4
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39334
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.52e0

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 4.093e0

VQSLOD
type: SiteQuality
SIO_000300: -3.995e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

QD
type: SiteQuality
SIO_000300: 9.5e-1

DP
type: SiteQuality
SIO_000300: 1.287146e6

MQ
type: SiteQuality
SIO_000300: 3.249e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 946
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 436
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 932
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 325
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 144
bin: 1.25e1
variant carriers: 2

Latino
type: Population
allele count: 3
allele frequency: 3.947368421052631e-4
allele num: 7600
num of homozygotes: 1

African
type: Population
allele count: 7
allele frequency: 1.451077943615257e-3
allele num: 4824
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 115
allele frequency: 2.912719720378907e-3
allele num: 39482
num of homozygotes: 34

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11832
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.190000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.290904e6

QD
type: SiteQuality
SIO_000300: 1.411e1

MQ
type: SiteQuality
SIO_000300: 3.008e1

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18690
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9185
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 951
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.016053647632595e-4
allele num: 39368
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

FS
type: SiteQuality
SIO_000300: 2.028e0

VQSLOD
type: SiteQuality
SIO_000300: -4.618e0

DP
type: SiteQuality
SIO_000300: 1.286683e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

MQ
type: SiteQuality
SIO_000300: 2.877e1

QD
type: SiteQuality
SIO_000300: 7.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.495e0

GenotypeQuality
all individuals: 4239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 307
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.052545155993432e-4
allele num: 4872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11880
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.96078431372549e-3
allele num: 510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.535239833688267e-5
allele num: 39444
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.897e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

QD
type: SiteQuality
SIO_000300: 4.83e0

MQRankSum
type: SiteQuality
SIO_000300: -1.356e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 2.801e1

DP
type: SiteQuality
SIO_000300: 1.295255e6

FS
type: SiteQuality
SIO_000300: 1.318e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11892
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 3.143e1

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.296866e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.536e0

QD
type: SiteQuality
SIO_000300: 1.161e1

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9250
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19003
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.034901365705615e-4
allele num: 6590
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.509e1

VQSLOD
type: SiteQuality
SIO_000300: -4.658e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
SIO_000300: 1.29968e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

MQ
type: SiteQuality
SIO_000300: 2.985e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 738
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4128
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 3.259452411994785e-4
allele num: 39884
num of homozygotes: 5

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.303166e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 1.155e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.678e0

MQ
type: SiteQuality
SIO_000300: 3.159e1

QD
type: SiteQuality
SIO_000300: 1.346e1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.766e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 692
bin: 2.25e1
variant carriers: 373

GenotypeQuality
all individuals: 688
bin: 5.25e1
variant carriers: 623

GenotypeQuality
all individuals: 5339
bin: 6.25e1
variant carriers: 660

GenotypeQuality
all individuals: 829
bin: 9.25e1
variant carriers: 790

GenotypeQuality
all individuals: 1516
bin: 6.75e1
variant carriers: 788

GenotypeQuality
all individuals: 601
bin: 7.25e1
variant carriers: 470

South Asian
type: Population
allele count: 9339
allele frequency: 7.561943319838057e-1
allele num: 12350
num of homozygotes: 3765

East Asian
type: Population
allele count: 4731
allele frequency: 7.023456057007126e-1
allele num: 6736
num of homozygotes: 1733

African
type: Population
allele count: 5038
allele frequency: 8.461538461538461e-1
allele num: 5954
num of homozygotes: 2244

European (Finnish)
type: Population
allele count: 2843
allele frequency: 6.553711387736284e-1
allele num: 4338
num of homozygotes: 1150

Latino
type: Population
allele count: 5980
allele frequency: 7.602339181286549e-1
allele num: 7866
num of homozygotes: 2559

European (Non-Finnish)
type: Population
allele count: 25727
allele frequency: 6.231410163251465e-1
allele num: 41286
num of homozygotes: 9340

Other
type: Population
allele count: 368
allele frequency: 6.690909090909091e-1
allele num: 550
num of homozygotes: 141

FS
type: SiteQuality
SIO_000300: 3.281e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.205e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

QD
type: SiteQuality
SIO_000300: 1.836e1

VQSLOD
type: SiteQuality
SIO_000300: 3.303e1

MQ
type: SiteQuality
SIO_000300: 2.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.678e0

DP
type: SiteQuality
SIO_000300: 2.496312e6

GenotypeQuality
all individuals: 22834
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 454
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4145
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.66333998669328e-4
allele num: 6012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6740
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.42914979757085e-4
allele num: 12350
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.834187373102581e-5
allele num: 41372
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 3.158e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 2.686e0

QD
type: SiteQuality
SIO_000300: 1.509e1

VQSLOD
type: SiteQuality
SIO_000300: -7.397e0

DP
type: SiteQuality
SIO_000300: 1.466844e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.301e0

GenotypeQuality
all individuals: 6249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.089305937550558e-5
allele num: 12362
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.267105930055753e-4
allele num: 7892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.831851565519907e-5
allele num: 41392
num of homozygotes: 1

African
type: Population
allele count: 1
allele frequency: 1.667222407469156e-4
allele num: 5998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6740
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.473296e6

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.334e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.359e0

QD
type: SiteQuality
SIO_000300: 1.388e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

FS
type: SiteQuality
SIO_000300: 6.35e-1

MQ
type: SiteQuality
SIO_000300: 3.139e1

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4142
bin: 9.75e1
variant carriers: 11

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7892
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.454898157129001e-3
allele num: 12372
num of homozygotes: 6

East Asian
type: Population
allele count: 5
allele frequency: 7.416196974191634e-4
allele num: 6742
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41424
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.669e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

QD
type: SiteQuality
SIO_000300: 8.27e0

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 1.47476e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

MQ
type: SiteQuality
SIO_000300: 2.87e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6285
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.413709872073377e-5
allele num: 41430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 2.837e1

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.204e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.47481e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

QD
type: SiteQuality
SIO_000300: 4.7e0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.824857666698833e-5
allele num: 41452
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.946e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

MQ
type: SiteQuality
SIO_000300: 3.157e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.501e0

DP
type: SiteQuality
SIO_000300: 1.476592e6

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24473
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.077544426494346e-5
allele num: 12380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

FS
type: SiteQuality
SIO_000300: 6.152e0

VQSLOD
type: SiteQuality
SIO_000300: -5.529e0

MQ
type: SiteQuality
SIO_000300: 2.97e1

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.97e-1

DP
type: SiteQuality
SIO_000300: 1.47732e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

GenotypeQuality
all individuals: 1269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24473
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.615508885298869e-4
allele num: 12380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.447946329456055e-4
allele num: 41438
num of homozygotes: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.529e0

FS
type: SiteQuality
SIO_000300: 6.152e0

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

QD
type: SiteQuality
SIO_000300: 4.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

MQ
type: SiteQuality
SIO_000300: 2.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

DP
type: SiteQuality
SIO_000300: 1.47732e6

GenotypeQuality
all individuals: 6298
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 7.596859964547987e-4
allele num: 7898
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.623188405797101e-3
allele num: 552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12386
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.025e1

QD
type: SiteQuality
SIO_000300: 5.05e0

VQSLOD
type: SiteQuality
SIO_000300: -4.537e0

FS
type: SiteQuality
SIO_000300: 1.184e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.847e0

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

DP
type: SiteQuality
SIO_000300: 1.478643e6

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.483679525222552e-3
allele num: 6740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41474
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.764e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.480597e6

MQ
type: SiteQuality
SIO_000300: 2.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

QD
type: SiteQuality
SIO_000300: 4.36e0

MQRankSum
type: SiteQuality
SIO_000300: -1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4097
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1256
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.410567929804262e-5
allele num: 41484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.176e1

VQSLOD
type: SiteQuality
SIO_000300: -6.688e0

MQRankSum
type: SiteQuality
SIO_000300: -2.179e0

DP
type: SiteQuality
SIO_000300: 1.480838e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 2.75e0

FS
type: SiteQuality
SIO_000300: 7.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.945e0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4095
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.411498022571622e-5
allele num: 41468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.147e0

FS
type: SiteQuality
SIO_000300: 1.921e0

DP
type: SiteQuality
SIO_000300: 1.480853e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.512e0

MQ
type: SiteQuality
SIO_000300: 3.169e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e0

QD
type: SiteQuality
SIO_000300: 4.39e0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 3.221649484536082e-4
allele num: 6208
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.195e1

VQSLOD
type: SiteQuality
SIO_000300: -4.387e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

QD
type: SiteQuality
SIO_000300: 1.72e0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

DP
type: SiteQuality
SIO_000300: 1.481283e6

GenotypeQuality
all individuals: 4095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.420955793347214e-5
allele num: 41306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6728
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.474247e6

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.452e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.487e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

QD
type: SiteQuality
SIO_000300: 2.18e0

MQ
type: SiteQuality
SIO_000300: 2.922e1

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4090
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.433326844461748e-5
allele num: 41096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.51e0

DP
type: SiteQuality
SIO_000300: 1.46047e6

MQ
type: SiteQuality
SIO_000300: 3.019e1

FS
type: SiteQuality
SIO_000300: 4.011e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

GenotypeQuality
all individuals: 687
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.430724355858046e-4
allele num: 12342
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 6.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

QD
type: SiteQuality
SIO_000300: 7.15e0

DP
type: SiteQuality
SIO_000300: 1.460543e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.98e-1

MQ
type: SiteQuality
SIO_000300: 2.99e1

VQSLOD
type: SiteQuality
SIO_000300: -4.137e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

GenotypeQuality
all individuals: 383
bin: 9.25e1
variant carriers: 70

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 58

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 81

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 100

GenotypeQuality
all individuals: 4575
bin: 9.75e1
variant carriers: 2653

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 50

Latino
type: Population
allele count: 232
allele frequency: 2.954661232806928e-2
allele num: 7852
num of homozygotes: 58

African
type: Population
allele count: 2768
allele frequency: 4.310183743382124e-1
allele num: 6422
num of homozygotes: 831

South Asian
type: Population
allele count: 533
allele frequency: 4.327001136548141e-2
allele num: 12318
num of homozygotes: 77

Other
type: Population
allele count: 35
allele frequency: 6.433823529411764e-2
allele num: 544
num of homozygotes: 14

European (Non-Finnish)
type: Population
allele count: 1295
allele frequency: 3.157150519284217e-2
allele num: 41018
num of homozygotes: 348

East Asian
type: Population
allele count: 103
allele frequency: 1.537772469393849e-2
allele num: 6698
num of homozygotes: 19

European (Finnish)
type: Population
allele count: 150
allele frequency: 3.467406380027739e-2
allele num: 4326
num of homozygotes: 37

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 2.901e1

VQSLOD
type: SiteQuality
SIO_000300: 6.968000000000001e1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

QD
type: SiteQuality
SIO_000300: 8.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.586e-1

FS
type: SiteQuality
SIO_000300: 1.885e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

DP
type: SiteQuality
SIO_000300: 1.547327e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
all individuals: 3046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24937
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.480286738351254e-4
allele num: 6696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.816e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

DP
type: SiteQuality
SIO_000300: 1.365077e6

QD
type: SiteQuality
SIO_000300: 8.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.199e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

FS
type: SiteQuality
SIO_000300: 6.204e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.58e-1

MQ
type: SiteQuality
SIO_000300: 2.909e1

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24635
bin: 6.25e1
variant carriers: 1

East Asian
type: Population
allele count: 2
allele frequency: 2.990430622009569e-4
allele num: 6688
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.611343860779891e-4
allele num: 6206
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.27420998980632e-4
allele num: 7848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.462629808395495e-4
allele num: 41022
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 2.271989613761766e-3
allele num: 12324
num of homozygotes: 6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: -1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

MQ
type: SiteQuality
SIO_000300: 2.863e1

DP
type: SiteQuality
SIO_000300: 1.362239e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

QD
type: SiteQuality
SIO_000300: 5.5e0

GenotypeQuality
all individuals: 3169
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.437716347325825e-5
allele num: 41022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

MQ
type: SiteQuality
SIO_000300: 2.863e1

QD
type: SiteQuality
SIO_000300: 5.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.42e0

DP
type: SiteQuality
SIO_000300: 1.362239e6

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3024
bin: 7.5e0
variant carriers: 16

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1161
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 5

Other
type: Population
allele count: 6
allele frequency: 1.123595505617977e-2
allele num: 534
num of homozygotes: 3

African
type: Population
allele count: 17
allele frequency: 2.757949383517197e-3
allele num: 6164
num of homozygotes: 3

Latino
type: Population
allele count: 10
allele frequency: 1.276161306789178e-3
allele num: 7836
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 408
allele frequency: 9.96726437680168e-3
allele num: 40934
num of homozygotes: 111

East Asian
type: Population
allele count: 1
allele frequency: 1.496110113704369e-4
allele num: 6684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 21
allele frequency: 4.865616311399444e-3
allele num: 4316
num of homozygotes: 7

South Asian
type: Population
allele count: 7
allele frequency: 5.691056910569106e-4
allele num: 12300
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

DP
type: SiteQuality
SIO_000300: 1.360792e6

VQSLOD
type: SiteQuality
SIO_000300: 2.002e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

MQ
type: SiteQuality
SIO_000300: 2.977e1

FS
type: SiteQuality
SIO_000300: 1.147e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.531e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 9.75e1
variant carriers: 99

GenotypeQuality
all individuals: 3024
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 7.75e1
variant carriers: 2

Latino
type: Population
allele count: 10
allele frequency: 1.276161306789178e-3
allele num: 7836
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4316
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.878048780487805e-4
allele num: 12300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 1.294767186202179e-3
allele num: 40934
num of homozygotes: 13

East Asian
type: Population
allele count: 1
allele frequency: 1.496110113704369e-4
allele num: 6684
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.745318352059925e-3
allele num: 534
num of homozygotes: 0

African
type: Population
allele count: 59
allele frequency: 9.571706683971446e-3
allele num: 6164
num of homozygotes: 6

VQSLOD
type: SiteQuality
SIO_000300: 2.002e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 1.360792e6

MQ
type: SiteQuality
SIO_000300: 2.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 1.147e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.531e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3789
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1216
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.625487646293888e-4
allele num: 6152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6682
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.891649953529325e-5
allele num: 40886
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

DP
type: SiteQuality
SIO_000300: 1.332692e6

QD
type: SiteQuality
SIO_000300: 5.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.859e0

MQ
type: SiteQuality
SIO_000300: 2.801e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24392
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.130081300813008e-5
allele num: 12300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.332185e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

MQ
type: SiteQuality
SIO_000300: 3.216e1

QD
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

FS
type: SiteQuality
SIO_000300: 7.476e0

VQSLOD
type: SiteQuality
SIO_000300: -4.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

GenotypeQuality
all individuals: 316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 328
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.600660066006601e-4
allele num: 6060
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6642
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.180628272251309e-5
allele num: 12224
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.087e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 2.792e1

DP
type: SiteQuality
SIO_000300: 1.297064e6

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

FS
type: SiteQuality
SIO_000300: 3.959e0

QD
type: SiteQuality
SIO_000300: 6.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

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

GenotypeQuality
all individuals: 463
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7782
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.505570611261668e-4
allele num: 6642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.087e0

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 3.959e0

MQ
type: SiteQuality
SIO_000300: 2.792e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.297064e6

QD
type: SiteQuality
SIO_000300: 6.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

GenotypeQuality
all individuals: 508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21749
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.188666885031116e-5
allele num: 12212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.904912836767037e-5
allele num: 40384
num of homozygotes: 1

African
type: Population
allele count: 2
allele frequency: 3.307972213033411e-4
allele num: 6046
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.284686536485098e-4
allele num: 7784
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.881e0

DP
type: SiteQuality
SIO_000300: 1.29018e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.091e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-3

FS
type: SiteQuality
SIO_000300: 9.148999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 2.916e1

QD
type: SiteQuality
SIO_000300: 4.67e0

GenotypeQuality
all individuals: 5846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2827
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4218
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.665001665001665e-4
allele num: 6006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12186
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 2.619e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.367e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

DP
type: SiteQuality
SIO_000300: 1.271396e6

MQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

QD
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
all individuals: 501
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5819
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.993757802746567e-5
allele num: 40050
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.139999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.777e0

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

DP
type: SiteQuality
SIO_000300: 1.267808e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

MQ
type: SiteQuality
SIO_000300: 3.2e1

QD
type: SiteQuality
SIO_000300: 1.928e1

GenotypeQuality
all individuals: 954
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.507007585271513e-4
allele num: 39814
num of homozygotes: 1

Latino
type: Population
allele count: 4
allele frequency: 5.197505197505198e-4
allele num: 7696
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.945525291828794e-3
allele num: 514
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.516990291262136e-4
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 42
allele frequency: 7.070707070707071e-3
allele num: 5940
num of homozygotes: 5

South Asian
type: Population
allele count: 141
allele frequency: 1.162024064611835e-2
allele num: 12134
num of homozygotes: 45

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.323e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.785e0

MQ
type: SiteQuality
SIO_000300: 2.688e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 1.249377e6

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

GenotypeQuality
all individuals: 115
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 201
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.707067258449983e-4
allele num: 5858
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.286377195889956e-5
allele num: 12068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.541554414680018e-5
allele num: 39346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4122
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.571e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.23e0

MQ
type: SiteQuality
SIO_000300: 2.934e1

DP
type: SiteQuality
SIO_000300: 1.221137e6

FS
type: SiteQuality
SIO_000300: 4.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

QD
type: SiteQuality
SIO_000300: 3.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

GenotypeQuality
all individuals: 1716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.311303435615001e-4
allele num: 7626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12068
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.86e0

DP
type: SiteQuality
SIO_000300: 1.221137e6

MQ
type: SiteQuality
SIO_000300: 2.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.23e0

VQSLOD
type: SiteQuality
SIO_000300: -4.571e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 3.45e0

GenotypeQuality
all individuals: 1070
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.694280584765324e-5
allele num: 38990
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.620000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.045e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

QD
type: SiteQuality
SIO_000300: 1.45e1

FS
type: SiteQuality
SIO_000300: 8.742000000000001e0

DP
type: SiteQuality
SIO_000300: 1.203505e6

MQ
type: SiteQuality
SIO_000300: 2.931e1

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.567657782570739e-5
allele num: 38946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 1.055130572408336e-3
allele num: 7582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.3236224404861e-5
allele num: 12014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4064
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.544163063619518e-4
allele num: 6476
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.935e0

MQ
type: SiteQuality
SIO_000300: 2.896e1

VQSLOD
type: SiteQuality
SIO_000300: -4.734e0

DP
type: SiteQuality
SIO_000300: 1.202348e6

QD
type: SiteQuality
SIO_000300: 6.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.332e0

GenotypeQuality
all individuals: 13529
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.947481243301179e-4
allele num: 37320
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3814
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.186743148502231e-4
allele num: 6276
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.902587519025875e-4
allele num: 5256
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 1.117414474815197e-3
allele num: 11634
num of homozygotes: 3

Latino
type: Population
allele count: 2
allele frequency: 2.74649821477616e-4
allele num: 7282
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.137186e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

QD
type: SiteQuality
SIO_000300: 8.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

FS
type: SiteQuality
SIO_000300: 5.9278e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

VQSLOD
type: SiteQuality
SIO_000300: -2.117e1

MQ
type: SiteQuality
SIO_000300: 2.469e1

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13995
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36768
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

MQ
type: SiteQuality
SIO_000300: 2.408e1

VQSLOD
type: SiteQuality
SIO_000300: -5.882e0

MQRankSum
type: SiteQuality
SIO_000300: -8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 1.119409e6

QD
type: SiteQuality
SIO_000300: 1.533e1

GenotypeQuality
all individuals: 2959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5073
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10205
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5856
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.737226277372263e-4
allele num: 10960
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.506e0

DP
type: SiteQuality
SIO_000300: 1.04933e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.43e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.38e-1

FS
type: SiteQuality
SIO_000300: 1.516e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.494e0

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.101e0

MQ
type: SiteQuality
SIO_000300: 2.627e1

GenotypeQuality
all individuals: 568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 1.25e1
variant carriers: 0