2-234591005-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591005
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591005
    reference: chr 2
allele count: 50
allele frequency: 4.120652711389484e-4
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.422G>C
  hgvsp: ENSP00000362525.3:p.Cys141Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44982G>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63797G>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44982G>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9570G>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9570G>C
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20510
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54490
  bin: 9.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys141Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum

2-234591008-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591008
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591008
    reference: chr 2
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9573T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9573T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44985T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.425T>C
  hgvsp: ENSP00000362525.3:p.Phe142Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63800T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44985T>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20510
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54486
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe142Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

2-234591009-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591009
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591009
    reference: chr 2
allele count: 6
allele frequency: 4.944049836022347e-5
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63801T>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44986T>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.426T>A
  hgvsp: ENSP00000362525.3:p.Phe142Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9574T>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44986T>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9574T>A
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20511
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 367
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 435
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54486
  bin: 9.75e1
  variant carriers: 6
hgvs: p.Phe142Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

2-234591012-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591012
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591012
    reference: chr 2
allele count: 11
allele frequency: 9.063195188267282e-5
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63804T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44989T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44989T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9577T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9577T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.429T>C
  hgvsp: ENST00000373426.3:c.429T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
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genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20512
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  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2441
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
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genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp143Asp
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

2-234591015-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591015
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591015
    reference: chr 2
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.432A>G
  hgvsp: ENST00000373426.3:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44992A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.2A>G
  hgvsp: ENST00000485022.1:c.2A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63807A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44992A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9580A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9580A>G
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala144Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

2-234591018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591018
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591018
    reference: chr 2
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.435G>A
  hgvsp: ENST00000373426.3:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44995G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63810G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9583G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.5G>A
  hgvsp: ENST00000485022.1:c.5G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44995G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9583G>A
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54489
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val145Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

2-234591022-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591022
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591022
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+44999C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9587C>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.9C>G
  hgvsp: ENSP00000420181.1:p.Leu4Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63814C>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+44999C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.439C>G
  hgvsp: ENSP00000362525.3:p.Leu147Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9587C>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu147Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-234591024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591024
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591024
    reference: chr 2
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9589C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45001C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.441C>T
  hgvsp: ENST00000373426.3:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.11C>T
  hgvsp: ENST00000485022.1:c.11C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63816C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45001C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9589C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20512
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu147Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-234591025-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591025
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591025
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63817G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9590G>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.12G>A
  hgvsp: ENSP00000420181.1:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45002G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9590G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45002G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.442G>A
  hgvsp: ENSP00000362525.3:p.Asp148Asn
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp148Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

2-234591029-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591029
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591029
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.446C>T
  hgvsp: ENSP00000362525.3:p.Pro149Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45006C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9594C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63821C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9594C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.16C>T
  hgvsp: ENSP00000420181.1:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45006C>T
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54490
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro149Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

2-234591032-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591032
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591032
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45009T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9597T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.449T>C
  hgvsp: ENSP00000362525.3:p.Phe150Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.19T>C
  hgvsp: ENSP00000420181.1:p.Phe7Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45009T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9597T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63824T>C
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20514
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54490
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe150Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-234591037-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591037
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591037
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9602G>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63829G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45014G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.454G>A
  hgvsp: ENSP00000362525.3:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.24G>A
  hgvsp: ENSP00000420181.1:p.Ala9Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45014G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9602G>A
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54491
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala152Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-234591038-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591038
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591038
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.25C>A
  hgvsp: ENSP00000420181.1:p.Ala9Asp
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63830C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45015C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45015C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.455C>A
  hgvsp: ENSP00000362525.3:p.Ala152Asp
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9603C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9603C>A
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala152Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

2-234591047-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591047
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591047
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9612T>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9612T>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.464T>G
  hgvsp: ENSP00000362525.3:p.Leu155Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.34T>G
  hgvsp: ENSP00000420181.1:p.Leu12Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45024T>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45024T>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63839T>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu155Ter
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

2-234591047-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591047
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591046
    reference: chr 2
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.466delA
  hgvsp: ENSP00000362525.3:p.Ile156LeufsTer40
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45026delA
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9614delA
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.36delA
  hgvsp: ENSP00000420181.1:p.Ile13LeufsTer40
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63841delA
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9614delA
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45026delA
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20517
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54491
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile156LeufsTer40
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TA
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD

2-234591050-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591050
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591050
    reference: chr 2
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.467T>C
  hgvsp: ENSP00000362525.3:p.Ile156Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63842T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45027T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9615T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45027T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9615T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.37T>C
  hgvsp: ENSP00000420181.1:p.Ile13Thr
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20517
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54492
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile156Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

2-234591057-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591057
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591057
    reference: chr 2
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45034C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45034C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63849C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.474C>T
  hgvsp: ENST00000373426.3:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.44C>T
  hgvsp: ENST00000485022.1:c.44C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9622C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9622C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20519
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala158Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

2-234591060-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591060
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591060
    reference: chr 2
allele count: 21
allele frequency: 1.729818780889621e-4
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63852A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45037A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9625A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45037A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9625A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.47A>G
  hgvsp: ENST00000485022.1:c.47A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.477A>G
  hgvsp: ENST00000373426.3:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20528
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2454
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys159Lys
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/2-234591068-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591068
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591068
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63860C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.485C>A
  hgvsp: ENSP00000362525.3:p.Ser162Tyr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.55C>A
  hgvsp: ENSP00000420181.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45045C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45045C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9633C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9633C>A
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20522
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54490
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser162Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

2-234591070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591070
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591070
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9635C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.57C>T
  hgvsp: ENSP00000420181.1:p.Leu20Phe
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9635C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.487C>T
  hgvsp: ENSP00000362525.3:p.Leu163Phe
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63862C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45047C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45047C>T
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20522
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2453
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54490
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu163Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

2-234591072-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591072
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591072
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.489C>T
  hgvsp: ENST00000373426.3:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.59C>T
  hgvsp: ENST00000485022.1:c.59C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9637C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63864C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45049C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9637C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45049C>T
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54490
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu163Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

2-234591075-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591075
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591075
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63867C>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.62C>G
  hgvsp: ENST00000485022.1:c.62C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9640C>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45052C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45052C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.492C>G
  hgvsp: ENST00000373426.3:c.492C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9640C>G
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro164Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-234591075-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591075
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591075
    reference: chr 2
allele count: 30
allele frequency: 2.471210398853359e-4
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.492C>T
  hgvsp: ENST00000373426.3:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45052C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.62C>T
  hgvsp: ENST00000485022.1:c.62C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45052C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9640C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9640C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63867C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20543
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54493
  bin: 9.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro164Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-234591084-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591084
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591083
    reference: chr 2
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.503delT
  hgvsp: ENSP00000362525.3:p.Phe168SerfsTer28
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9651delT
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45063delT
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63878delT
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.73delT
  hgvsp: ENSP00000420181.1:p.Phe25SerfsTer28
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9651delT
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45063delT
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20535
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe168SerfsTer28
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: CT
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-234591090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591090
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591090
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9655C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63882C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.507C>T
  hgvsp: ENST00000373426.3:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.77C>T
  hgvsp: ENST00000485022.1:c.77C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45067C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45067C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9655C>T
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala169Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-234591097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591097
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591097
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9662A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45074A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.514A>G
  hgvsp: ENSP00000362525.3:p.Ile172Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45074A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63889A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9662A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.84A>G
  hgvsp: ENSP00000420181.1:p.Ile29Val
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20535
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile172Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-234591100-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591100
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591100
    reference: chr 2
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.517T>G
  hgvsp: ENSP00000362525.3:p.Phe173Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45077T>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9665T>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9665T>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.87T>G
  hgvsp: ENSP00000420181.1:p.Phe30Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45077T>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63892T>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe173Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-234591101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591101
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591101
    reference: chr 2
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9666T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.88T>C
  hgvsp: ENSP00000420181.1:p.Phe30Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.518T>C
  hgvsp: ENSP00000362525.3:p.Phe173Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45078T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63893T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9666T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45078T>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe173Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

2-234591106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591106
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591106
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.523C>T
  hgvsp: ENSP00000362525.3:p.His175Tyr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9671C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45083C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45083C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.93C>T
  hgvsp: ENSP00000420181.1:p.His32Tyr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63898C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9671C>T
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20537
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His175Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/2-234591126-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591126
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63918A>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45103A>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9691A>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45103A>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9691A>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.113A>C
  hgvsp: ENST00000485022.1:c.113A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.543A>C
  hgvsp: ENST00000373426.3:c.543A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala181Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-234591127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591127
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591127
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63919C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9692C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.114C>T
  hgvsp: ENSP00000420181.1:p.Gln39Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45104C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.544C>T
  hgvsp: ENSP00000362525.3:p.Gln182Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45104C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9692C>T
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54494
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln182Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

2-234591148-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591148
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591148
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.135T>C
  hgvsp: ENSP00000420181.1:p.Tyr46His
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9713T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45125T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9713T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.565T>C
  hgvsp: ENSP00000362525.3:p.Tyr189His
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63940T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45125T>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20541
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr189His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

2-234591154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591154
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591154
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9719C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45131C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.571C>T
  hgvsp: ENSP00000362525.3:p.Pro191Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45131C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.141C>T
  hgvsp: ENSP00000420181.1:p.Pro48Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63946C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9719C>T
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro191Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-234591158-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591158
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591158
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.145G>C
  hgvsp: ENSP00000420181.1:p.Arg49Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9723G>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63950G>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.575G>C
  hgvsp: ENSP00000362525.3:p.Arg192Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9723G>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45135G>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45135G>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg192Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-234591160-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591160
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591160
    reference: chr 2
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.577C>A
  hgvsp: ENSP00000362525.3:p.Leu193Ile
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9725C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63952C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45137C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45137C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9725C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.147C>A
  hgvsp: ENSP00000420181.1:p.Leu50Ile
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20545
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu193Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

2-234591169-GGGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591169
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591166
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.587_589delGGT
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45147_855+45149delGGT
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45147_855+45149delGGT
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9735_855+9737delGGT
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63962_855+63964delGGT
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9735_855+9737delGGT
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.157_159delGGT
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly196_Phe197delinsVal
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: GGGT
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

2-234591180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591180
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591180
    reference: chr 2
allele count: 6
allele frequency: 4.942176534545814e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.167C>T
  hgvsp: ENST00000485022.1:c.167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45157C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9745C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45157C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.597C>T
  hgvsp: ENST00000373426.3:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9745C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63972C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20548
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp199Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

2-234591181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591181
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591181
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.168G>A
  hgvsp: ENSP00000420181.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45158G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63973G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9746G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.598G>A
  hgvsp: ENSP00000362525.3:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9746G>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45158G>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala200Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

2-234591185-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591185
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591185
    reference: chr 2
allele count: 11
allele frequency: 9.060209208467177e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.172T>C
  hgvsp: ENSP00000420181.1:p.Met58Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9750T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.602T>C
  hgvsp: ENSP00000362525.3:p.Met201Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45162T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45162T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63977T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9750T>C
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20550
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54494
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met201Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

2-234591188-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591188
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591188
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9753C>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45165C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9753C>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45165C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.175C>G
  hgvsp: ENSP00000420181.1:p.Thr59Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.605C>G
  hgvsp: ENSP00000362525.3:p.Thr202Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63980C>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20551
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54494
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr202Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

2-234591195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591195
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591195
    reference: chr 2
allele count: 17
allele frequency: 1.40026028367626e-4
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.612G>A
  hgvsp: ENST00000373426.3:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9760G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45172G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.182G>A
  hgvsp: ENST00000485022.1:c.182G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63987G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45172G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9760G>A
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20562
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys204Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-234591205-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591205
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591205
    reference: chr 2
allele count: 42642
allele frequency: 3.512925708071771e-1
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9770T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9770T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45182T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.622T>C
  hgvsp: ENSP00000362525.3:p.Trp208Arg
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63997T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.192T>C
  hgvsp: ENSP00000420181.1:p.Trp65Arg
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45182T>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 7.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 6.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42399
  bin: 9.75e1
  variant carriers: 33335
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 9.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 7.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 6.25e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57672
  bin: 9.75e1
  variant carriers: 34579
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 2
hgvs: p.Trp208Arg
num of homozygotes: 8031
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

2-234591206-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591206
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591206
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.623G>A
  hgvsp: ENSP00000362525.3:p.Trp208Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.193G>A
  hgvsp: ENSP00000420181.1:p.Trp65Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9771G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+63998G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45183G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45183G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9771G>A
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24215
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Trp208Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-234591210-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591210
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591210
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.627C>A
  hgvsp: ENSP00000362525.3:p.Asn209Lys
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9775C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45187C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64002C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.197C>A
  hgvsp: ENSP00000420181.1:p.Asn66Lys
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9775C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45187C>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24216
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5197
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn209Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

2-234591211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591211
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591211
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45188C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45188C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.198C>T
  hgvsp: ENSP00000420181.1:p.His67Tyr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9776C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9776C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.628C>T
  hgvsp: ENSP00000362525.3:p.His210Tyr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64003C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24216
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His210Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

2-234591217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591217
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591217
    reference: chr 2
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9782A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45194A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45194A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.634A>G
  hgvsp: ENSP00000362525.3:p.Met212Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64009A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.204A>G
  hgvsp: ENSP00000420181.1:p.Met69Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9782A>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24215
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met212Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

2-234591219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591219
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591219
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.206G>A
  hgvsp: ENSP00000420181.1:p.Met69Ile
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45196G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9784G>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64011G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.636G>A
  hgvsp: ENSP00000362525.3:p.Met212Ile
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45196G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9784G>A
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24213
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met212Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-234591221-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591221
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591221
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64013A>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9786A>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.638A>C
  hgvsp: ENSP00000362525.3:p.His213Pro
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9786A>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45198A>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.208A>C
  hgvsp: ENSP00000420181.1:p.His70Pro
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45198A>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His213Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

2-234591221-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591221
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591221
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45198A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.208A>G
  hgvsp: ENSP00000420181.1:p.His70Arg
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9786A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.638A>G
  hgvsp: ENSP00000362525.3:p.His213Arg
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9786A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45198A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64013A>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5192
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His213Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

2-234591226-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591226
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591226
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.643G>A
  hgvsp: ENSP00000362525.3:p.Glu215Lys
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.213G>A
  hgvsp: ENSP00000420181.1:p.Glu72Lys
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9791G>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64018G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9791G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45203G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45203G>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52485
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu215Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/2-234591237-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591237
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591237
    reference: chr 2
allele count: 3
allele frequency: 2.471495419495156e-5
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9802A>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.224A>C
  hgvsp: ENSP00000420181.1:p.Leu75Phe
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.654A>C
  hgvsp: ENSP00000362525.3:p.Leu218Phe
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9802A>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45214A>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64029A>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45214A>C
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24213
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52487
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu218Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

2-234591237-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591237
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591237
    reference: chr 2
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45214A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.224A>G
  hgvsp: ENST00000485022.1:c.224A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9802A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64029A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9802A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45214A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.654A>G
  hgvsp: ENST00000373426.3:c.654A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24213
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5172
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52487
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu218Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

2-234591237-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591237
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591237
    reference: chr 2
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45214A>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.654A>T
  hgvsp: ENSP00000362525.3:p.Leu218Phe
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64029A>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45214A>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9802A>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.224A>T
  hgvsp: ENSP00000420181.1:p.Leu75Phe
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9802A>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24213
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu218Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

2-234591243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591243
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591243
    reference: chr 2
allele count: 66
allele frequency: 5.437379512613073e-4
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9808C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.660C>T
  hgvsp: ENST00000373426.3:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.230C>T
  hgvsp: ENST00000485022.1:c.230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45220C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9808C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45220C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64035C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24219
  bin: 9.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys220Cys
num of homozygotes: 1
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-234591245-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591245
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591245
    reference: chr 2
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9810C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64037C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45222C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.662C>A
  hgvsp: ENSP00000362525.3:p.Pro221His
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9810C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.232C>A
  hgvsp: ENSP00000420181.1:p.Pro78His
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45222C>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24197
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52485
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro221His
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

2-234591249-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591249
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591249
    reference: chr 2
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9814T>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.666T>A
  hgvsp: ENSP00000362525.3:p.Tyr222Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45226T>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64041T>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.236T>A
  hgvsp: ENSP00000420181.1:p.Tyr79Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45226T>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9814T>A
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24196
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5152
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr222Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

2-234591250-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591250
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591250
    reference: chr 2
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9815T>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.237T>A
  hgvsp: ENSP00000420181.1:p.Phe80Ile
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9815T>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64042T>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.667T>A
  hgvsp: ENSP00000362525.3:p.Phe223Ile
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45227T>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45227T>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24195
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52484
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5146
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe223Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

2-234591254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591254
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591254
    reference: chr 2
allele count: 4
allele frequency: 3.295598727898891e-5
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.241T>C
  hgvsp: ENSP00000420181.1:p.Phe81Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45231T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.671T>C
  hgvsp: ENSP00000362525.3:p.Phe224Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9819T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45231T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64046T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9819T>C
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24194
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52484
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Phe224Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/2-234591255-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591255
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591255
    reference: chr 2
allele count: 10
allele frequency: 8.238996819747228e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.672C>A
  hgvsp: ENSP00000362525.3:p.Phe224Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45232C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64047C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.242C>A
  hgvsp: ENSP00000420181.1:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9820C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9820C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45232C>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24193
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe224Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-234591255-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591255
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591255
    reference: chr 2
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.672C>G
  hgvsp: ENSP00000362525.3:p.Phe224Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64047C>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9820C>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45232C>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9820C>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.242C>G
  hgvsp: ENSP00000420181.1:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45232C>G
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24193
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5148
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe224Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-234591272-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591272
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591271
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.690delA
  hgvsp: ENSP00000362525.3:p.Ile230MetfsTer36
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64065delA
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9838delA
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9838delA
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45250delA
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.260delA
  hgvsp: ENSP00000420181.1:p.Ile87MetfsTer36
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45250delA
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24188
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile230MetfsTer36
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: TA
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS

2-234591273-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591273
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591273
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64065A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9838A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45250A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9838A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.260A>G
  hgvsp: ENSP00000420181.1:p.Ile87Met
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.690A>G
  hgvsp: ENSP00000362525.3:p.Ile230Met
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45250A>G
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24187
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile230Met
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

2-234591284-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591284
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591284
    reference: chr 2
allele count: 6
allele frequency: 4.943723942455053e-5
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.271T>C
  hgvsp: ENSP00000420181.1:p.Ile91Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45261T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9849T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45261T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.701T>C
  hgvsp: ENSP00000362525.3:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64076T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9849T>C
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24187
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5156
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile234Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

2-234591285-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591285
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591285
    reference: chr 2
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.272T>C
  hgvsp: ENST00000485022.1:c.272T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64077T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9850T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45262T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45262T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9850T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.702T>C
  hgvsp: ENST00000373426.3:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24184
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile234Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

2-234591287-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591287
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591287
    reference: chr 2
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45264T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45264T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9852T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64079T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.704T>C
  hgvsp: ENSP00000362525.3:p.Leu235Pro
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9852T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.274T>C
  hgvsp: ENSP00000420181.1:p.Leu92Pro
  variant of: http://identifiers.org/hgnc/12539
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu235Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-234591295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591295
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591295
    reference: chr 2
allele count: 8
allele frequency: 6.592066448029797e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.282C>T
  hgvsp: ENSP00000420181.1:p.Pro95Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64087C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45272C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45272C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.712C>T
  hgvsp: ENSP00000362525.3:p.Pro238Ser
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9860C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9860C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24187
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro238Ser
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-234591302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591302
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591302
    reference: chr 2
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9867C>T
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.289C>T
  hgvsp: ENSP00000420181.1:p.Thr97Met
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45279C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9867C>T
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.719C>T
  hgvsp: ENSP00000362525.3:p.Thr240Met
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45279C>T
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64094C>T
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24185
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr240Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

2-234591303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591303
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591303
    reference: chr 2
allele count: 4
allele frequency: 3.29614186594591e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45280G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9868G>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45280G>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.290G>A
  hgvsp: ENST00000485022.1:c.290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.720G>A
  hgvsp: ENST00000373426.3:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9868G>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64095G>A
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24187
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr240Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

2-234591312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591312
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591312
    reference: chr 2
allele count: 23
allele frequency: 1.895344046147507e-4
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.729T>C
  hgvsp: ENST00000373426.3:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45289T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45289T>C
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9877T>C
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.299T>C
  hgvsp: ENST00000485022.1:c.299T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9877T>C
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64104T>C
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24191
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp243Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-234591327-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591327
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591327
    reference: chr 2
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45304A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.314A>G
  hgvsp: ENST00000485022.1:c.314A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45304A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9892A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.744A>G
  hgvsp: ENST00000373426.3:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64119A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9892A>G
  variant of: http://identifiers.org/hgnc/12541
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24179
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr248Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-234591329-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591329
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591329
    reference: chr 2
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64121C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.316C>A
  hgvsp: ENSP00000420181.1:p.Ser106Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9894C>A
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9894C>A
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.746C>A
  hgvsp: ENSP00000362525.3:p.Ser249Ter
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45306C>A
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45306C>A
  variant of: http://identifiers.org/hgnc/12531
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24177
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52477
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser249Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

2-234591331-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 234591331
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 234591331
    reference: chr 2
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000362544
  ensembl transcript: ENST00000373445
  gene symbol: UGT1A10
  hgvsc: ENST00000373445.1:c.855+45308A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241119
  ensembl protein: ENSP00000346768
  ensembl transcript: ENST00000354728
  gene symbol: UGT1A9
  hgvsc: ENST00000354728.4:c.855+9896A>G
  variant of: http://identifiers.org/hgnc/12541
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000242515
  ensembl protein: ENSP00000343838
  ensembl transcript: ENST00000344644
  gene symbol: UGT1A10
  hgvsc: ENST00000344644.5:c.855+45308A>G
  variant of: http://identifiers.org/hgnc/12531
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000362549
  ensembl transcript: ENST00000373450
  gene symbol: UGT1A8
  hgvsc: ENST00000373450.4:c.855+64123A>G
  variant of: http://identifiers.org/hgnc/12540
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000362525
  ensembl transcript: ENST00000373426
  gene symbol: UGT1A7
  hgvsc: ENST00000373426.3:c.748A>G
  hgvsp: ENSP00000362525.3:p.Ile250Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244122
  ensembl protein: ENSP00000420181
  ensembl transcript: ENST00000485022
  gene symbol: UGT1A7
  hgvsc: ENST00000485022.1:c.318A>G
  hgvsp: ENSP00000420181.1:p.Ile107Val
  variant of: http://identifiers.org/hgnc/12539
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241635
  ensembl protein: ENSP00000476286
  ensembl transcript: ENST00000609637
  gene symbol: UGT1A8
  hgvsc: ENST00000609637.1:c.855+9896A>G
  variant of: http://identifiers.org/hgnc/12540
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24178
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile250Val
num of homozygotes: 0
reference allele: A

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

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

GenotypeQuality
all individuals: 433
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.747002398081535e-4
allele num: 66720
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.824392126592049e-4
allele num: 10364
num of homozygotes: 0

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

Latino
type: Population
allele count: 16
allele frequency: 1.382408847416624e-3
allele num: 11574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.644e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e0

QD
type: SiteQuality
SIO_000300: 8.6e0

MQ
type: SiteQuality
SIO_000300: 5.347e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 7.037e0

DP
type: SiteQuality
SIO_000300: 5.139622e6

MQRankSum
type: SiteQuality
SIO_000300: -3.715e0

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 367
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.055e0

QD
type: SiteQuality
SIO_000300: 1.587e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQ
type: SiteQuality
SIO_000300: 5.283e1

FS
type: SiteQuality
SIO_000300: 2.513e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 5.139429e6

GenotypeQuality
all individuals: 2439
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 848
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493780162465154e-5
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 5.139805e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.411e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.951e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.677e0

MQ
type: SiteQuality
SIO_000300: 5.758e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.83e0

QD
type: SiteQuality
SIO_000300: 1.615e1

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54488
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 847
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.99199712256092e-5
allele num: 66726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.796e1

DP
type: SiteQuality
SIO_000300: 5.140355e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -9.729e-1

QD
type: SiteQuality
SIO_000300: 1.711e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.962e0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54486
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2456
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 846
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.64e-1

MQ
type: SiteQuality
SIO_000300: 5.127e1

MQRankSum
type: SiteQuality
SIO_000300: -5.589e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.773e0

FS
type: SiteQuality
SIO_000300: 1.4577e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -5.786e0

DP
type: SiteQuality
SIO_000300: 5.140272e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

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

GenotypeQuality
all individuals: 374
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 846
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.108e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.624e1

QD
type: SiteQuality
SIO_000300: 7.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

FS
type: SiteQuality
SIO_000300: 9.96e-1

DP
type: SiteQuality
SIO_000300: 5.140387e6

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

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

GenotypeQuality
all individuals: 849
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54490
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 374
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.707e0

MQRankSum
type: SiteQuality
SIO_000300: 8.960000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -9.295e0

FS
type: SiteQuality
SIO_000300: 5.948e0

MQ
type: SiteQuality
SIO_000300: 5.591e1

DP
type: SiteQuality
SIO_000300: 5.140456e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

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

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 848
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54490
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 376
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.152e1

MQ
type: SiteQuality
SIO_000300: 5.199e1

MQRankSum
type: SiteQuality
SIO_000300: -3.384e0

FS
type: SiteQuality
SIO_000300: 3.427e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.285e0

DP
type: SiteQuality
SIO_000300: 5.140424e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-1

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

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

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

GenotypeQuality
all individuals: 847
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54490
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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QD
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SIO_000300: 1.479e1

MQRankSum
type: SiteQuality
SIO_000300: -1.014e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: -9.848e-1

FS
type: SiteQuality
SIO_000300: 9.162000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

DP
type: SiteQuality
SIO_000300: 5.140515e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

African
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allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

QD
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SIO_000300: 1.335e1

FS
type: SiteQuality
SIO_000300: 1.1424e1

InbreedingCoeff
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SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 5.140623e6

MQ
type: SiteQuality
SIO_000300: 5.829e1

VQSLOD
type: SiteQuality
SIO_000300: -1.023e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 5.140772e6

QD
type: SiteQuality
SIO_000300: 3.48e0

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.473e0

VQSLOD
type: SiteQuality
SIO_000300: -1.858e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.77e-1

MQ
type: SiteQuality
SIO_000300: 5.498e1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.367e1

DP
type: SiteQuality
SIO_000300: 5.140953e6

MQRankSum
type: SiteQuality
SIO_000300: -8.467000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.33e0

FS
type: SiteQuality
SIO_000300: 5.0148e1

VQSLOD
type: SiteQuality
SIO_000300: -1.998e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.15e0

FS
type: SiteQuality
SIO_000300: 4.9853e1

MQRankSum
type: SiteQuality
SIO_000300: -8.474e0

DP
type: SiteQuality
SIO_000300: 5.140961e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.371e1

VQSLOD
type: SiteQuality
SIO_000300: -1.981e1

QD
type: SiteQuality
SIO_000300: 4.14e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.788e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
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Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 2.885170225043277e-4
allele num: 10398
num of homozygotes: 0

Other
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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FS
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.824e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.112e0

ClippingRankSum
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
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BaseQRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.032e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 21
allele frequency: 2.426623526692859e-3
allele num: 8654
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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allele num: 10396
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Other
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num of homozygotes: 0

FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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QD
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MQ
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SIO_000300: 5.502e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 1.816860465116279e-3
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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DP
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QD
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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allele num: 10396
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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ClippingRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66734
num of homozygotes: 0

East Asian
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African
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European (Finnish)
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South Asian
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Latino
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Other
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InbreedingCoeff
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FS
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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European (Finnish)
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Other
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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Latino
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European (Finnish)
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East Asian
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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Other
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66738
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Other
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African
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European (Finnish)
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Latino
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East Asian
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QD
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BaseQRankSum
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MQ
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FS
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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Other
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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FS
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11578
num of homozygotes: 0

European (Finnish)
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Other
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East Asian
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African
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European (Non-Finnish)
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South Asian
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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Other
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African
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East Asian
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele num: 66740
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DP
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648186994306263e-4
allele num: 66740
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.576e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.176e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 5.147097e6

VQSLOD
type: SiteQuality
SIO_000300: -9.965000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

GenotypeQuality
all individuals: 745
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 647
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 442
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

FS
type: SiteQuality
SIO_000300: 6.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.137e0

QD
type: SiteQuality
SIO_000300: 1.77e1

DP
type: SiteQuality
SIO_000300: 5.147268e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
all individuals: 849
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 375
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54498
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.547274416374479e-4
allele num: 66738
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

DP
type: SiteQuality
SIO_000300: 5.149745e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

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

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

GenotypeQuality
all individuals: 350
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 215
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 132
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 6

African
type: Population
allele count: 2735
allele frequency: 2.629302057296674e-1
allele num: 10402
num of homozygotes: 357

European (Finnish)
type: Population
allele count: 3058
allele frequency: 4.624924379915306e-1
allele num: 6612
num of homozygotes: 704

Latino
type: Population
allele count: 2150
allele frequency: 1.857932941583132e-1
allele num: 11572
num of homozygotes: 235

European (Non-Finnish)
type: Population
allele count: 25858
allele frequency: 3.874902595456453e-1
allele num: 66732
num of homozygotes: 5059

East Asian
type: Population
allele count: 1672
allele frequency: 1.933395004625347e-1
allele num: 8648
num of homozygotes: 167

Other
type: Population
allele count: 327
allele frequency: 3.601321585903084e-1
allele num: 908
num of homozygotes: 67

South Asian
type: Population
allele count: 6842
allele frequency: 4.143653100775194e-1
allele num: 16512
num of homozygotes: 1442

DP
type: SiteQuality
SIO_000300: 1.0551761e7

MQRankSum
type: SiteQuality
SIO_000300: -6.052e0

MQ
type: SiteQuality
SIO_000300: 5.62e1

VQSLOD
type: SiteQuality
SIO_000300: -2.474e0

QD
type: SiteQuality
SIO_000300: 1.86e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.57e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

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

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

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

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

GenotypeQuality
all individuals: 52484
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.589e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: -1.63e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 6.202094e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.79e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

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

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

GenotypeQuality
all individuals: 475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52486
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.48e0

VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.41e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.104e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.178e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.609e0

DP
type: SiteQuality
SIO_000300: 6.202109e6

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 52485
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.876e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.552e0

MQRankSum
type: SiteQuality
SIO_000300: 5.49e0

MQ
type: SiteQuality
SIO_000300: 5.813e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

FS
type: SiteQuality
SIO_000300: 2.996e0

DP
type: SiteQuality
SIO_000300: 6.202106e6

QD
type: SiteQuality
SIO_000300: 1.371e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.62e-1

GenotypeQuality
all individuals: 473
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52484
bin: 9.75e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5195
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 4.319e0

QD
type: SiteQuality
SIO_000300: 8.26e0

VQSLOD
type: SiteQuality
SIO_000300: -1.369e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.199e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.542e0

DP
type: SiteQuality
SIO_000300: 6.202075e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 5.621e1

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 52485
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 473
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5199
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1071
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.756e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.83e0

MQ
type: SiteQuality
SIO_000300: 5.633e1

QD
type: SiteQuality
SIO_000300: 1.244e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.325e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.624000000000001e0

DP
type: SiteQuality
SIO_000300: 6.201486e6

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

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

GenotypeQuality
all individuals: 5192
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52485
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.52e-1

DP
type: SiteQuality
SIO_000300: 6.201426e6

FS
type: SiteQuality
SIO_000300: 2.455e0

MQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

MQ
type: SiteQuality
SIO_000300: 5.538e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.091e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.301e1

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

GenotypeQuality
all individuals: 1071
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52485
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.301e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

DP
type: SiteQuality
SIO_000300: 6.201426e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.52e-1

FS
type: SiteQuality
SIO_000300: 2.455e0

VQSLOD
type: SiteQuality
SIO_000300: -1.091e0

MQ
type: SiteQuality
SIO_000300: 5.538e1

MQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.775e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.45e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.148e0

DP
type: SiteQuality
SIO_000300: 6.201168e6

MQRankSum
type: SiteQuality
SIO_000300: -5.329e0

FS
type: SiteQuality
SIO_000300: 2.531e0

VQSLOD
type: SiteQuality
SIO_000300: -4.348e0

MQ
type: SiteQuality
SIO_000300: 5.693e1

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 5172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.873e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 6.200935e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.220000000000001e0

QD
type: SiteQuality
SIO_000300: 1.488e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.488e1

MQ
type: SiteQuality
SIO_000300: 5.787e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.220000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.873e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

DP
type: SiteQuality
SIO_000300: 6.200935e6

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

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

GenotypeQuality
all individuals: 1069
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
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variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52487
bin: 9.75e1
variant carriers: 2

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.488e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.220000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.200935e6

VQSLOD
type: SiteQuality
SIO_000300: -1.873e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

GenotypeQuality
all individuals: 5162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52485
bin: 9.75e1
variant carriers: 65

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

European (Finnish)
type: Population
allele count: 37
allele frequency: 5.594194133655882e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.8472950696838e-4
allele num: 66730
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.777675063554426e-4
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

FS
type: SiteQuality
SIO_000300: 5.24e-1

VQSLOD
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SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.266999999999999e0

DP
type: SiteQuality
SIO_000300: 6.205851e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

QD
type: SiteQuality
SIO_000300: 1.416e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.865e0

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

FS
type: SiteQuality
SIO_000300: 5.216e0

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.445e1

DP
type: SiteQuality
SIO_000300: 6.198089e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.0203e1

QD
type: SiteQuality
SIO_000300: 1.489e1

DP
type: SiteQuality
SIO_000300: 6.197871e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 4.93e0

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.689e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.912e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 6.19767e6

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5143
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994305409860632e-5
allele num: 66730
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

FS
type: SiteQuality
SIO_000300: 2.513e0

QD
type: SiteQuality
SIO_000300: 1.421e1

MQ
type: SiteQuality
SIO_000300: 5.804e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e0

VQSLOD
type: SiteQuality
SIO_000300: -1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -6.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.68e-1

DP
type: SiteQuality
SIO_000300: 6.197519e6

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

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5148
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52484
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.926782273603083e-4
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 7
allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

FS
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.014e0

DP
type: SiteQuality
SIO_000300: 6.196999e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.187e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.706e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

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

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52484
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.706e0

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

FS
type: SiteQuality
SIO_000300: 5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 6.196999e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.187e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.014e0

GenotypeQuality
all individuals: 463
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
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variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.01e1

DP
type: SiteQuality
SIO_000300: 6.195798e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 6.016e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.441e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

FS
type: SiteQuality
SIO_000300: 8.218999999999999e0

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

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

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5140
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52481
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

VQSLOD
type: SiteQuality
SIO_000300: 7.03e-1

FS
type: SiteQuality
SIO_000300: 5.408e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.189e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

DP
type: SiteQuality
SIO_000300: 6.195563e6

QD
type: SiteQuality
SIO_000300: 5.67e0

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

GenotypeQuality
all individuals: 52482
bin: 9.75e1
variant carriers: 6

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

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

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

GenotypeQuality
all individuals: 1048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
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variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 6
allele frequency: 6.933210076265311e-4
allele num: 8654
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

DP
type: SiteQuality
SIO_000300: 6.19639e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.949999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 7.92e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52480
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.524e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.19521e6

MQ
type: SiteQuality
SIO_000300: 5.924e1

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

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52480
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
SIO_000300: -1.015e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.55e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.194828e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52482
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.74893945237177e-4
allele num: 10372
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

FS
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 6.195807e6

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 438
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variant carriers: 0

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

GenotypeQuality
all individuals: 52479
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.877e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.004e0

DP
type: SiteQuality
SIO_000300: 6.194779e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

GenotypeQuality
all individuals: 52479
bin: 9.75e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5152
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49667246237784e-5
allele num: 66716
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.718e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 6.195315e6

MQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.162e0

QD
type: SiteQuality
SIO_000300: 1.129e1

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

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

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52479
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.495577609210566e-5
allele num: 66706
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 5.781460782424359e-4
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.036448436690275e-3
allele num: 11578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.409e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.947e1

FS
type: SiteQuality
SIO_000300: 5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

DP
type: SiteQuality
SIO_000300: 6.198091e6

GenotypeQuality
all individuals: 1044
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52477
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 460
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5127
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

DP
type: SiteQuality
SIO_000300: 6.193454e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.361e1

FS
type: SiteQuality
SIO_000300: 1.101e0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.882e0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 351
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.739e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 6.077e0

VQSLOD
type: SiteQuality
SIO_000300: -3.302e-1

DP
type: SiteQuality
SIO_000300: 6.193121e6

QD
type: SiteQuality
SIO_000300: 1.139e1