9-86153161-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153161
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153161
    reference: chr 9
allele count: 3
allele frequency: 1.89873417721519e-4
allele num: 15800
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-15C>G
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-15C>G
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2563
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32685
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8201
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 82
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-86153163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153163
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153163
    reference: chr 9
allele count: 1
allele frequency: 6.341958396752917e-5
allele num: 15768
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-17C>T
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33077
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
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genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 822
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 464
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

9-86153164-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153164
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153164
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 15660
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-18T>C
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-18T>C
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33612
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8500
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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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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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 640
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genotype quality: GenotypeQuality
  all individuals: 812
  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1586
  num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

9-86153165-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153165
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153165
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 15700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-19C>T
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-19C>T
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9474
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33791
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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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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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 152
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

9-86153165-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153165
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153165
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 15700
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-19C>A
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-19C>A
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9474
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
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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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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 500
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

9-86153166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153166
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153166
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 15488
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-20G>A
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 33876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 47
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 458
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

9-86153171-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153171
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153171
    reference: chr 9
allele count: 1
allele frequency: 7.517666516313337e-5
allele num: 13302
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-25C>G
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-25C>G
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

9-86153186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86153186
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86153186
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 9608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000365621
  ensembl transcript: ENST00000376438
  gene symbol: FRMD3
  hgvsc: ENST00000376438.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/24125
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172159
  ensembl protein: ENSP00000303508
  ensembl transcript: ENST00000304195
  gene symbol: FRMD3
  hgvsc: ENST00000304195.3:c.-40C>T
  variant of: http://identifiers.org/hgnc/24125
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 230
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

9-86238047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238047
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238047
    reference: chr 9
allele count: 17
allele frequency: 1.460481099656357e-2
allele num: 1164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-764C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 4273
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 15
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 1252
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 7
num of homozygotes: 1
population: East Asian
  type: Population
  allele count: 3
  allele frequency: 1.153846153846154e-1
  allele num: 26
  num of homozygotes: 1
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

9-86238048-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238048
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238048
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.-39G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-763G>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
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genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3618
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 507
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 1394
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 24
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-86238053-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238053
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238053
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.-34C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-758C>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 6
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 20
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genotype quality: GenotypeQuality
  all individuals: 462
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 270
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 56
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

9-86238067-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238067
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238067
    reference: chr 9
allele count: 8
allele frequency: 6.211180124223602e-3
allele num: 1288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-332G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-744G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
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  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 5
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

9-86238073-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238073
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238073
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-326G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-738G>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

9-86238086-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238086
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238086
    reference: chr 9
allele count: 2791
allele frequency: 8.015508328546812e-1
allele num: 3482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.-1T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.-1T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.-1T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-725T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.-1T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-313T>C
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 2.5e0
  variant carriers: 1235
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.25e1
  variant carriers: 1089
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 7.5e0
  variant carriers: 2395
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 1.75e1
  variant carriers: 1008
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 8.25e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 2.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 1.25e1
  variant carriers: 568
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 6.25e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.75e1
  variant carriers: 293
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 9.75e1
  variant carriers: 569
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.25e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 663
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.25e1
  variant carriers: 410
num of homozygotes: 1087
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/9-86238101-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238101
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238101
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.15C>A
  hgvsp: ENST00000533522.1:c.15C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-710C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.15C>A
  hgvsp: ENST00000376419.4:c.15C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.15C>A
  hgvsp: ENST00000405990.3:c.15C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-298C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.15C>A
  hgvsp: ENST00000376417.4:c.15C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4728
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1869
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly5Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-86238111-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238111
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238111
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 1494
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.25G>C
  hgvsp: ENSP00000365601.4:p.Val9Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.25G>C
  hgvsp: ENSP00000434673.1:p.Val9Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-288G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.25G>C
  hgvsp: ENSP00000385324.2:p.Val9Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.25G>C
  hgvsp: ENSP00000365599.4:p.Val9Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-700G>C
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5431
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val9Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-86238156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238156
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238156
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+37G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+37G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+20G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+20G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+20G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+20G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5031
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

9-86238160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238160
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238160
    reference: chr 9
allele count: 2
allele frequency: 2.169197396963124e-3
allele num: 922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+41G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+24G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+41G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+24G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+24G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+24G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

9-86238215-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238215
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238215
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+79C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+79C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+79C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+79C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+96C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+96C>G
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4500
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

9-86238216-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238216
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238216
    reference: chr 9
allele count: 2
allele frequency: 5.128205128205128e-3
allele num: 390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+80C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+80C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+80C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+97C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+97C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+80C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4547
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

9-86238217-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238217
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238217
    reference: chr 9
allele count: 1
allele frequency: 2.631578947368421e-3
allele num: 380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+81G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+98G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+81G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+98G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+81G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+81G>C
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4467
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/9-86238239-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238239
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238239
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+103C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+103C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+120C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+103C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+120C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+103C>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4671
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

9-86238251-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238251
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238251
    reference: chr 9
allele count: 2
allele frequency: 4.761904761904762e-3
allele num: 420
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+115C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+132C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+132C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+115C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+115C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+115C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

9-86238352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238352
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238352
    reference: chr 9
allele count: 1
allele frequency: 1.0351966873706e-3
allele num: 966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.93G>A
  hgvsp: ENST00000454393.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+216G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+216G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+216G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+233G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+216G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+233G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg31Arg
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

9-86238400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238400
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238400
    reference: chr 9
allele count: 1
allele frequency: 2.272727272727273e-2
allele num: 44
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+264G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+281G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+264G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.141G>A
  hgvsp: ENST00000454393.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+264G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+264G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+281G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 2.5e0
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genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4631
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu47Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

9-86238432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238432
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238432
    reference: chr 9
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.173C>T
  hgvsp: ENSP00000403290.1:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+296C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+296C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+313C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+313C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+296C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+296C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro58Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

9-86238460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86238460
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86238460
    reference: chr 9
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.179+22C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.50+324C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.50+324C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.50+324C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-263+324C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-692+341C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.33+341C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum

9-86241324-TTTTTTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241324
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241317
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 6
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-691-14_-691-8delTTGTTTT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.34-14_34-8delTTGTTTT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4382
  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: TTTTTTTG
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

9-86241361-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241361
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241361
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1561T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1735T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-687T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.38T>A
  hgvsp: ENSP00000434673.1:p.Leu13His
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1735T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2427T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1735T>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
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: 189
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu13His
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

9-86241371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241371
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241371
    reference: chr 9
allele count: 12
allele frequency: 6.896551724137931e-2
allele num: 174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2417G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.48G>A
  hgvsp: ENST00000533522.1:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1725G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1551G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-677G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1725G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1725G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 2.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.5e0
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 2.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4677
  bin: 7.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser16Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

9-86241371-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241371
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241371
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 174
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1725G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1725G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-677G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.48G>T
  hgvsp: ENST00000533522.1:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1551G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1725G>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2417G>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4677
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser16Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

9-86241386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241386
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241386
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1710C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-662C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1536C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2402C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.63C>T
  hgvsp: ENST00000533522.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1710C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1710C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr21Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

9-86241390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241390
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241390
    reference: chr 9
allele count: 117
allele frequency: 2.28515625e-1
allele num: 512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1706G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.67G>A
  hgvsp: ENSP00000434673.1:p.Gly23Ser
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1532G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1706G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-658G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2398G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1706G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 2.5e0
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 7.5e0
  variant carriers: 479
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 3419
  bin: 7.5e0
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 1.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 1.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly23Ser
num of homozygotes: 10
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum

9-86241392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241392
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241392
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-656C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1704C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1704C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1704C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2396C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.69C>T
  hgvsp: ENST00000533522.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1530C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly23Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-86241410-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241410
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241410
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1686C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1686C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1512C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2378C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.87C>A
  hgvsp: ENSP00000434673.1:p.Cys29Ter
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-638C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1686C>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: stop gained
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3468
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys29Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

9-86241435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241435
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241435
    reference: chr 9
allele count: 1
allele frequency: 5.070993914807302e-4
allele num: 1972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1487G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1661G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2353G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-613G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.112G>A
  hgvsp: ENSP00000434673.1:p.Asp38Asn
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1661G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1661G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp38Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

9-86241443-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241443
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241443
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 2440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.120T>C
  hgvsp: ENST00000533522.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1653T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-605T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1479T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1653T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2345T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1653T>C
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3565
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His40His
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-86241449-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241449
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241449
    reference: chr 9
allele count: 1
allele frequency: 3.450655624568668e-4
allele num: 2898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1473A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1647A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2339A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-599A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1647A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1647A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.126A>T
  hgvsp: ENST00000533522.1:c.126A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser42Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

9-86241457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241457
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241457
    reference: chr 9
allele count: 1
allele frequency: 2.95159386068477e-4
allele num: 3388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1639G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2331G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1639G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-591G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1639G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.134G>A
  hgvsp: ENSP00000434673.1:p.Gly45Glu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1465G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly45Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

9-86241476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241476
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241476
    reference: chr 9
allele count: 1
allele frequency: 2.354048964218456e-4
allele num: 4248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-572C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1620C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.153C>T
  hgvsp: ENST00000533522.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1446C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2312C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1620C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1620C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2930
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly51Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

9-86241489-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241489
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241489
    reference: chr 9
allele count: 7643
allele frequency: 8.356658648589548e-1
allele num: 9146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1433A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.166A>G
  hgvsp: ENSP00000434673.1:p.Thr56Ala
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-559A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1607A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1607A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2299A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1607A>G
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 2.25e1
  variant carriers: 960
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 2.5e0
  variant carriers: 493
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 1.25e1
  variant carriers: 1463
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 1.75e1
  variant carriers: 1578
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 736
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.75e1
  variant carriers: 342
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.75e1
  variant carriers: 490
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 5.25e1
  variant carriers: 484
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.25e1
  variant carriers: 162
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.25e1
  variant carriers: 247
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 6.75e1
  variant carriers: 234
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 1223
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.25e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.75e1
  variant carriers: 134
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.25e1
  variant carriers: 95
hgvs: p.Thr56Ala
num of homozygotes: 3178
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-86241491-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241491
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241491
    reference: chr 9
allele count: 25
allele frequency: 3.10096750186058e-3
allele num: 8062
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1605C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1605C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1431C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1605C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.168C>G
  hgvsp: ENST00000533522.1:c.168C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2297C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-557C>G
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr56Thr
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

9-86241524-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241524
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241525
    reference: chr 9
allele count: 2
allele frequency: 2.615062761506276e-4
allele num: 7648
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1394dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1568dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2260dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1568dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1568dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.205dupT
  hgvsp: ENSP00000434673.1:p.Cys69LeufsTer7
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-520dupT
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys69LeufsTer7
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

9-86241574-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241574
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241574
    reference: chr 9
allele count: 1
allele frequency: 1.697792869269949e-4
allele num: 5890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.251C>T
  hgvsp: ENSP00000434673.1:p.Pro84Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1522C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1522C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1522C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2214C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-474C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1348C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro84Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

9-86241575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241575
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241575
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 5638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2213G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1521G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1521G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.252G>A
  hgvsp: ENST00000533522.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1521G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-473G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1347G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro84Pro
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

9-86241583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241583
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241583
    reference: chr 9
allele count: 1
allele frequency: 1.790830945558739e-4
allele num: 5584
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1513C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-465C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1339C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1513C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1513C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.260C>T
  hgvsp: ENSP00000434673.1:p.Ser87Leu
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2205C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser87Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/9-86241584-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241584
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241584
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 5514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.261A>C
  hgvsp: ENST00000533522.1:c.261A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1512A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1512A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2204A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-464A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1338A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1512A>C
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser87Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

9-86241612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241612
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241612
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 4684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.289G>A
  hgvsp: ENSP00000434673.1:p.Val97Met
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1484G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1310G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1484G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1484G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-436G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2176G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val97Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

9-86241647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241647
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241647
    reference: chr 9
allele count: 1
allele frequency: 3.736920777279522e-4
allele num: 2676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1275G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-401G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1449G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1449G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2141G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1449G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

9-86241650-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86241650
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86241651
    reference: chr 9
allele count: 1
allele frequency: 4.351610095735422e-4
allele num: 2298
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*9dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-262-1269dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-2135dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-1443dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-1443dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-1443dupT
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-395dupT
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/9-86243059-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243059
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243059
    reference: chr 9
allele count: 1
allele frequency: 6.083465141744738e-5
allele num: 16438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-729C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-88-37C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-125C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-37C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-37C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-37C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*316-37C>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

9-86243071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243071
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243071
    reference: chr 9
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-25G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-88-25G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-25G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-25G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*316-25G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-717G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

9-86243071-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243071
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243071
    reference: chr 9
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-113G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*316-25G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-25G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-717G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-25G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-25G>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-88-25G>C
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1907
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4461
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

9-86243076-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243076
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243076
    reference: chr 9
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-88-20C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.51-20C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.51-20C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-108C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.180-20C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*316-20C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-712C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-86243099-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243099
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243099
    reference: chr 9
allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-85C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*319C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.183C>A
  hgvsp: ENST00000454393.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-689C>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.54C>A
  hgvsp: ENST00000376417.4:c.54C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.54C>A
  hgvsp: ENST00000376419.4:c.54C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-85C>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser18Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

9-86243108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243108
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243108
    reference: chr 9
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.63C>T
  hgvsp: ENST00000376417.4:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*328C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.63C>T
  hgvsp: ENST00000376419.4:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.192C>T
  hgvsp: ENST00000454393.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-680C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-76C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-76C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly21Gly
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

9-86243109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243109
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243109
    reference: chr 9
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-75G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-679G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.64G>A
  hgvsp: ENSP00000365601.4:p.Ala22Thr
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-75G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.64G>A
  hgvsp: ENSP00000365599.4:p.Ala22Thr
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.193G>A
  hgvsp: ENSP00000403290.1:p.Ala65Thr
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*329G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala22Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

9-86243114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243114
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243114
    reference: chr 9
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-70G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.69G>A
  hgvsp: ENST00000376419.4:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-674G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.198G>A
  hgvsp: ENST00000454393.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.69G>A
  hgvsp: ENST00000376417.4:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-70G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*334G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu23Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

9-86243152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243152
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243152
    reference: chr 9
allele count: 3
allele frequency: 1.816200508536142e-4
allele num: 16518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-636C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.81+26C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*346+26C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.210+26C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.81+26C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-58+26C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-58+26C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2398
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

9-86243153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243153
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243153
    reference: chr 9
allele count: 4
allele frequency: 2.42101440503571e-4
allele num: 16522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.210+27G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-58+27G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*346+27G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-58+27G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.81+27G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.81+27G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-635G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-86243746-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243746
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243746
    reference: chr 9
allele count: 2
allele frequency: 1.693279374163943e-5
allele num: 118114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-42C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-42C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-42C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-42C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-42C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-42C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-42C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16928
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13985
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-86243748-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243748
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243748
    reference: chr 9
allele count: 1
allele frequency: 8.447087444249223e-6
allele num: 118384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-40A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-40A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-40A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-40A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-40A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-40A>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-40A>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3297
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1755
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3771
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

9-86243749-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243749
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243749
    reference: chr 9
allele count: 1
allele frequency: 8.449799739746167e-6
allele num: 118346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-39T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-39T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-39T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-39T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-39T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-39T>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-39T>C
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11698
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

9-86243750-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243750
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243750
    reference: chr 9
allele count: 36
allele frequency: 3.041568097330179e-4
allele num: 118360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-38C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-38C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-38C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-38C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-38C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-38C>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-38C>G
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19056
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11734
  bin: 9.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

9-86243750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243750
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243750
    reference: chr 9
allele count: 1
allele frequency: 8.448800270361608e-6
allele num: 118360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-38C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-38C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-38C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-38C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-38C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-38C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-38C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16200
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6619
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

9-86243756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243756
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243756
    reference: chr 9
allele count: 1
allele frequency: 8.418500496691529e-6
allele num: 118786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-32G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-32G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-32G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-32G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-32G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-32G>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-32G>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4042
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4653
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

9-86243757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243757
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243757
    reference: chr 9
allele count: 1
allele frequency: 8.413825598223e-6
allele num: 118852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-31C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-31C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-31C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-31C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-31C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-31C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-31C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4717
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18748
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

9-86243762-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243762
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243762
    reference: chr 9
allele count: 1
allele frequency: 8.380403265005112e-6
allele num: 119326
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-26T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-26T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-26T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-26T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-26T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-26T>A
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-26T>A
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22068
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1919
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

9-86243763-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243763
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243763
    reference: chr 9
allele count: 1
allele frequency: 8.376752835530836e-6
allele num: 119378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-25A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-25A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-25A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-25A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-25A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-25A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-25A>G
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4913
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11873
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

9-86243764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243764
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243764
    reference: chr 9
allele count: 2
allele frequency: 1.674565031733007e-5
allele num: 119434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-24C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-24C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-24C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-24C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-24C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-24C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-24C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7406
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

9-86243767-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243767
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243767
    reference: chr 9
allele count: 2
allele frequency: 1.670257720766314e-5
allele num: 119742
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-21C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-21C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-21C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-21C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-21C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-21C>T
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-21C>T
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11898
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-86243773-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243773
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243773
    reference: chr 9
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-15A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-15A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-15A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-15A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-15A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-15A>C
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-15A>C
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11946
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21566
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

9-86243773-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86243773
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 86243773
    reference: chr 9
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365599
  ensembl transcript: ENST00000376417
  gene symbol: IDNK
  hgvsc: ENST00000376417.4:c.82-15A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000434673
  ensembl transcript: ENST00000533522
  gene symbol: IDNK
  hgvsc: ENST00000533522.1:c.*347-15A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000385324
  ensembl transcript: ENST00000405990
  gene symbol: IDNK
  hgvsc: ENST00000405990.3:c.51-15A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000436381
  ensembl transcript: ENST00000530832
  gene symbol: IDNK
  hgvsc: ENST00000530832.1:c.-57-15A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000365601
  ensembl transcript: ENST00000376419
  gene symbol: IDNK
  hgvsc: ENST00000376419.4:c.82-15A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000403290
  ensembl transcript: ENST00000454393
  gene symbol: IDNK
  hgvsc: ENST00000454393.1:c.211-15A>G
  variant of: http://identifiers.org/hgnc/31367
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148057
  ensembl protein: ENSP00000277124
  ensembl transcript: ENST00000277124
  gene symbol: IDNK
  hgvsc: ENST00000277124.8:c.-57-15A>G
  variant of: http://identifiers.org/hgnc/31367
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11946
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21566
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.838709677419355e-4
allele num: 6200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

VQSLOD
type: SiteQuality
SIO_000300: -3.417e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.653e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.17e-2

FS
type: SiteQuality
SIO_000300: 4.736e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 2.9316e5

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6176
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.475361463558572e-4
allele num: 6778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.511e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.261e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.22e-2

MQ
type: SiteQuality
SIO_000300: 5.788e1

DP
type: SiteQuality
SIO_000300: 2.91384e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.633e0

MQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

QD
type: SiteQuality
SIO_000300: 1.821e1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.269e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.90511e5

VQSLOD
type: SiteQuality
SIO_000300: -1.856e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

QD
type: SiteQuality
SIO_000300: 1.157e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.89434e5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

QD
type: SiteQuality
SIO_000300: 1.157e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 2.89434e5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.245e0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 6.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 2.88603e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4940
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.626016260162602e-4
allele num: 6150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 2.50854e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 4.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.729999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.155e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3540
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.0247e5

VQSLOD
type: SiteQuality
SIO_000300: 2.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.44e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.026e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.19047619047619e-2
allele num: 672
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.60427807486631e-2
allele num: 374
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

DP
type: SiteQuality
SIO_000300: 3.5236e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 9.49e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 3.5528e4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.73e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.5762e4

QD
type: SiteQuality
SIO_000300: 1.23e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.12e-2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 2.941176470588235e-2
allele num: 34
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 9.900990099009901e-3
allele num: 606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.915708812260536e-3
allele num: 522
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 4.0866e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.58e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

FS
type: SiteQuality
SIO_000300: 8.821e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.239e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 9.23e0

VQSLOD
type: SiteQuality
SIO_000300: -9.776e-1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.006e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.77e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.2967e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 114

GenotypeQuality
all individuals: 870
bin: 2.25e1
variant carriers: 766

GenotypeQuality
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bin: 7.25e1
variant carriers: 56

GenotypeQuality
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bin: 3.75e1
variant carriers: 247

GenotypeQuality
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bin: 9.25e1
variant carriers: 55

GenotypeQuality
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bin: 5.75e1
variant carriers: 64

GenotypeQuality
all individuals: 63
bin: 6.75e1
variant carriers: 62

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

African
type: Population
allele count: 182
allele frequency: 9.191919191919192e-1
allele num: 198
num of homozygotes: 86

European (Non-Finnish)
type: Population
allele count: 976
allele frequency: 7.496159754224271e-1
allele num: 1302
num of homozygotes: 348

Other
type: Population
allele count: 25
allele frequency: 6.944444444444444e-1
allele num: 36
num of homozygotes: 8

East Asian
type: Population
allele count: 128
allele frequency: 8.888888888888888e-1
allele num: 144
num of homozygotes: 56

Latino
type: Population
allele count: 47
allele frequency: 7.34375e-1
allele num: 64
num of homozygotes: 18

South Asian
type: Population
allele count: 1428
allele frequency: 8.244803695150116e-1
allele num: 1732
num of homozygotes: 569

European (Finnish)
type: Population
allele count: 5
allele frequency: 8.333333333333334e-1
allele num: 6
num of homozygotes: 2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.104e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

DP
type: SiteQuality
SIO_000300: 6.4278e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 2.496e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.615e1

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 9.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.415e0

DP
type: SiteQuality
SIO_000300: 4.8141e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-2

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

FS
type: SiteQuality
SIO_000300: 2.198e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.950000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.695e0

DP
type: SiteQuality
SIO_000300: 4.754e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.142e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.42e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.0e1

DP
type: SiteQuality
SIO_000300: 3.4585e4

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.941176470588235e-2
allele num: 68
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

DP
type: SiteQuality
SIO_000300: 3.4597e4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.359999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

QD
type: SiteQuality
SIO_000300: 1.479e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.872e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

DP
type: SiteQuality
SIO_000300: 2.5895e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.08e-2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
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allele count: 2
allele frequency: 4.545454545454546e-2
allele num: 44
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.96e-2

FS
type: SiteQuality
SIO_000300: 1.0292e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: -2.907e-1

DP
type: SiteQuality
SIO_000300: 2.5892e4

QD
type: SiteQuality
SIO_000300: 1.338e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 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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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.941176470588235e-2
allele num: 34
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 14
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

QD
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MQRankSum
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SIO_000300: 3.58e-1

VQSLOD
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 6.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.920000000000001e-2

DP
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SIO_000300: 2.562e4

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

East Asian
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allele frequency: 0.0e0
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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: NaN
allele num: 0
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DP
type: SiteQuality
SIO_000300: 2.6977e4

QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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ClippingRankSum
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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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African
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Latino
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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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East Asian
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InbreedingCoeff
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FS
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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DP
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SIO_000300: 3.1633e4

GenotypeQuality
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variant carriers: 1

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

Latino
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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SIO_000300: 0.0e0

DP
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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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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European (Finnish)
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African
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Other
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Latino
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allele num: 0
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South Asian
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 8.333333333333333e-2
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num of homozygotes: 0

East Asian
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DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.16e0

MQ
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VQSLOD
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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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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European (Finnish)
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East Asian
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allele frequency: NaN
allele num: 0
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South Asian
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allele frequency: NaN
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African
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: NaN
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num of homozygotes: 0

Latino
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allele frequency: NaN
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Other
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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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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East Asian
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South Asian
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African
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European (Finnish)
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allele frequency: NaN
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Other
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European (Non-Finnish)
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allele frequency: NaN
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Latino
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DP
type: SiteQuality
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ClippingRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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FS
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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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Latino
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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DP
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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DP
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VQSLOD
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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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African
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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Other
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European (Finnish)
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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SIO_000300: 5.807e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10
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South Asian
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allele frequency: 0.0e0
allele num: 186
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 5.79e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

InbreedingCoeff
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SIO_000300: -7.530000000000001e-2

VQSLOD
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DP
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SIO_000300: 2.8878e4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

GenotypeQuality
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variant carriers: 23

GenotypeQuality
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variant carriers: 39

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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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: 10

GenotypeQuality
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GenotypeQuality
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variant carriers: 127

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

Other
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allele frequency: 5.0e-1
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.196969696969697e-1
allele num: 132
num of homozygotes: 3

Latino
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allele count: 2
allele frequency: 2.0e-1
allele num: 10
num of homozygotes: 0

European (Finnish)
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
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allele count: 5
allele frequency: 2.5e-1
allele num: 20
num of homozygotes: 0

South Asian
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allele count: 78
allele frequency: 2.5e-1
allele num: 312
num of homozygotes: 7

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.38e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
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SIO_000300: 0.0e0

QD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.719e1

VQSLOD
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SIO_000300: -3.331e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.12e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 8
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

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

African
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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: 44
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.347e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.370000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.533e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 3.5336e4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.845018450184502e-3
allele num: 542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.8173e4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.97e-2

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.123e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.445e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

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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allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.79e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.52e-2

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 1940
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.329787234042553e-3
allele num: 752
num of homozygotes: 0

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
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MQ
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MQRankSum
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 880
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Latino
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Other
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East Asian
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South Asian
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allele frequency: 4.401408450704225e-4
allele num: 2272
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.304e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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DP
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SIO_000300: 5.7477e4

QD
type: SiteQuality
SIO_000300: 1.156e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 1094
num of homozygotes: 0

European (Finnish)
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Other
type: Population
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allele num: 44
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East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2884
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

ReadPosRankSum
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.051e0

GenotypeQuality
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variant carriers: 375

GenotypeQuality
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variant carriers: 166

GenotypeQuality
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variant carriers: 225

GenotypeQuality
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variant carriers: 510

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 278

GenotypeQuality
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GenotypeQuality
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variant carriers: 44

GenotypeQuality
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variant carriers: 355

South Asian
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allele count: 5463
allele frequency: 8.541275797373359e-1
allele num: 6396
num of homozygotes: 2320

African
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allele count: 163
allele frequency: 9.157303370786517e-1
allele num: 178
num of homozygotes: 74

European (Non-Finnish)
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allele frequency: 7.785651018600531e-1
allele num: 2258
num of homozygotes: 679

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

Latino
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allele count: 66
allele frequency: 8.25e-1
allele num: 80
num of homozygotes: 27

East Asian
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allele count: 113
allele frequency: 8.560606060606061e-1
allele num: 132
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Other
type: Population
allele count: 80
allele frequency: 7.843137254901961e-1
allele num: 102
num of homozygotes: 31

QD
type: SiteQuality
SIO_000300: 2.561e1

BaseQRankSum
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SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.07e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

DP
type: SiteQuality
SIO_000300: 9.1719e4

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.233e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

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: 2.173913043478261e-2
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

East Asian
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allele frequency: 4.615384615384616e-2
allele num: 130
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 17
allele frequency: 3.020611229566453e-3
allele num: 5628
num of homozygotes: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.535e0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.32e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

DP
type: SiteQuality
SIO_000300: 8.4094e4

MQ
type: SiteQuality
SIO_000300: 5.904e1

QD
type: SiteQuality
SIO_000300: 1.436e1

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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allele frequency: 0.0e0
allele num: 66
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 152
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1848
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 2
allele frequency: 3.725782414307004e-4
allele num: 5368
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 2.505e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

DP
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SIO_000300: 8.1535e4

ClippingRankSum
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SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 2.87e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1414
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South Asian
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allele frequency: 2.440214738897023e-4
allele num: 4098
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

ClippingRankSum
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -3.37e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 2.09e-1

DP
type: SiteQuality
SIO_000300: 6.8433e4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.845e1

QD
type: SiteQuality
SIO_000300: 9.59e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.27e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.744e4

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.672e-1

QD
type: SiteQuality
SIO_000300: 5.74e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 2.592016588906169e-4
allele num: 3858
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.552e1

FS
type: SiteQuality
SIO_000300: 5.119e0

QD
type: SiteQuality
SIO_000300: 1.054e1

MQRankSum
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DP
type: SiteQuality
SIO_000300: 6.7661e4

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.67e-2

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1144
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3206
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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African
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MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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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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African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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Latino
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Other
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European (Non-Finnish)
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allele frequency: 1.506024096385542e-3
allele num: 664
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European (Finnish)
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allele frequency: 0.0e0
allele num: 2
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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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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variant carriers: 0

Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 540
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African
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East Asian
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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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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 920
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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Other
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allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 1.30821559392988e-4
allele num: 7644
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.962e0

VQSLOD
type: SiteQuality
SIO_000300: -1.918e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.235e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

DP
type: SiteQuality
SIO_000300: 3.53389e5

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.744e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.089324618736384e-3
allele num: 918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 1.644e0

QD
type: SiteQuality
SIO_000300: 1.345e1

DP
type: SiteQuality
SIO_000300: 3.55278e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.05761316872428e-3
allele num: 486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5326
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.644e0

VQSLOD
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SIO_000300: 2.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

DP
type: SiteQuality
SIO_000300: 3.55278e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.23e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.30582397492818e-4
allele num: 7658
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.42e-2

DP
type: SiteQuality
SIO_000300: 3.55754e5

VQSLOD
type: SiteQuality
SIO_000300: -1.019e0

QD
type: SiteQuality
SIO_000300: 1.638e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.118e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.746721618583739e-4
allele num: 5338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.34e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

DP
type: SiteQuality
SIO_000300: 3.57504e5

MQ
type: SiteQuality
SIO_000300: 5.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

FS
type: SiteQuality
SIO_000300: 2.958e0

VQSLOD
type: SiteQuality
SIO_000300: -1.266e0

QD
type: SiteQuality
SIO_000300: 1.452e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.304801670146138e-4
allele num: 7664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
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DP
type: SiteQuality
SIO_000300: 3.57983e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.51e-2

FS
type: SiteQuality
SIO_000300: 1.069e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

QD
type: SiteQuality
SIO_000300: 9.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.89e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.098901098901099e-3
allele num: 910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5342
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

FS
type: SiteQuality
SIO_000300: 5.94e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
SIO_000300: -3.668e-1

DP
type: SiteQuality
SIO_000300: 3.58051e5

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 2
allele frequency: 2.608922515001304e-4
allele num: 7666
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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East Asian
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allele count: 2
allele frequency: 4.11522633744856e-3
allele num: 486
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5342
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 3.424657534246575e-3
allele num: 292
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.69e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.907e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.067e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.871958068139274e-4
allele num: 5342
num of homozygotes: 0

East Asian
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allele frequency: 4.11522633744856e-3
allele num: 486
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 7666
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Latino
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allele frequency: 0.0e0
allele num: 292
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Other
type: Population
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.44e-1

InbreedingCoeff
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QD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.927e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 486
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African
type: Population
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allele frequency: 4.385964912280702e-3
allele num: 912
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Other
type: Population
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allele frequency: 0.0e0
allele num: 206
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5344
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South Asian
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allele frequency: 0.0e0
allele num: 7666
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 292
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MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
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QD
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.44e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.076923076923077e-5
allele num: 65000
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.783264e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4416
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GenotypeQuality
all individuals: 15856
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535013661621589e-5
allele num: 65146
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e0

VQSLOD
type: SiteQuality
SIO_000300: -5.723e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.373e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.798445e6

QD
type: SiteQuality
SIO_000300: 1.578e1

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
all individuals: 6620
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.235191420376606e-5
allele num: 16038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65108
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.851e1

MQRankSum
type: SiteQuality
SIO_000300: -7.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.171e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.801995e6

MQ
type: SiteQuality
SIO_000300: 5.878e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2162
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variant carriers: 0

African
type: Population
allele count: 25
allele frequency: 2.501000400160064e-3
allele num: 9996
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.861277445109781e-4
allele num: 16032
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65130
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.644e1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQ
type: SiteQuality
SIO_000300: 5.991e1

DP
type: SiteQuality
SIO_000300: 1.807874e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2162
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variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535390756947643e-5
allele num: 65130
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.807874e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e0

QD
type: SiteQuality
SIO_000300: 1.644e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

GenotypeQuality
all individuals: 7031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 1840
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2509
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GenotypeQuality
all individuals: 11793
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.218132073125233e-5
allele num: 16082
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.846039e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.006e0

FS
type: SiteQuality
SIO_000300: 6.042e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 2.55e1

VQSLOD
type: SiteQuality
SIO_000300: -2.336e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11813
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variant carriers: 1

GenotypeQuality
all individuals: 7056
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528070657987225e-5
allele num: 65442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16090
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.435e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

DP
type: SiteQuality
SIO_000300: 1.851169e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.488e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 249
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variant carriers: 0

GenotypeQuality
all individuals: 7355
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521838380763963e-5
allele num: 65710
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.134e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.872309e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 502
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variant carriers: 0

GenotypeQuality
all individuals: 7387
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.76e1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.195000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.874685e6

GenotypeQuality
all individuals: 997
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 223
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GenotypeQuality
all individuals: 2609
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variant carriers: 0

GenotypeQuality
all individuals: 475
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variant carriers: 0

GenotypeQuality
all individuals: 11878
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.334267040149393e-4
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65774
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.684e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.878475e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.918e1

QD
type: SiteQuality
SIO_000300: 1.278e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.482e0

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
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GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7498
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20997
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4321
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.033244358165494e-5
allele num: 65936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.887968e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

QD
type: SiteQuality
SIO_000300: 1.611e1

FS
type: SiteQuality
SIO_000300: 2.088e0

MQRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

GenotypeQuality
all individuals: 7606
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5076
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511258878645912e-5
allele num: 66170
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: -1.753e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.31e-1

FS
type: SiteQuality
SIO_000300: 1.25e1

DP
type: SiteQuality
SIO_000300: 1.900443e6

QD
type: SiteQuality
SIO_000300: 8.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4