9-5763502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763502
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763502
    reference: chr 9
allele count: 3
allele frequency: 2.471902705909495e-5
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2149G>A
  hgvsp: ENST00000545641.1:c.2149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2475G>A
  hgvsp: ENST00000251879.6:c.2475G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.106G>A
  hgvsp: ENST00000545243.1:c.106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2238G>A
  hgvsp: ENST00000418622.3:c.2238G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2127G>A
  hgvsp: ENST00000449720.2:c.2127G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2475G>A
  hgvsp: ENST00000414202.2:c.2475G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2238G>A
  hgvsp: ENST00000381532.2:c.2238G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3174G>A
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15941
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5363
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln825Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-5763514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763514
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763514
    reference: chr 9
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2487C>T
  hgvsp: ENST00000414202.2:c.2487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3186C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.118C>T
  hgvsp: ENST00000545243.1:c.118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2487C>T
  hgvsp: ENST00000251879.6:c.2487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2250C>T
  hgvsp: ENST00000418622.3:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2139C>T
  hgvsp: ENST00000449720.2:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2161C>T
  hgvsp: ENST00000545641.1:c.2161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2250C>T
  hgvsp: ENST00000381532.2:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15942
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His829His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

9-5763517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763517
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763517
    reference: chr 9
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2142C>T
  hgvsp: ENST00000449720.2:c.2142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2253C>T
  hgvsp: ENST00000418622.3:c.2253C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2164C>T
  hgvsp: ENST00000545641.1:c.2164C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2253C>T
  hgvsp: ENST00000381532.2:c.2253C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2490C>T
  hgvsp: ENST00000251879.6:c.2490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.121C>T
  hgvsp: ENST00000545243.1:c.121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2490C>T
  hgvsp: ENST00000414202.2:c.2490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3189C>T
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17723
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3584
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His830His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

9-5763523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763523
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763523
    reference: chr 9
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2170A>G
  hgvsp: ENST00000545641.1:c.2170A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.127A>G
  hgvsp: ENST00000545243.1:c.127A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2496A>G
  hgvsp: ENST00000251879.6:c.2496A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2259A>G
  hgvsp: ENST00000381532.2:c.2259A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2259A>G
  hgvsp: ENST00000418622.3:c.2259A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3195A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2148A>G
  hgvsp: ENST00000449720.2:c.2148A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2496A>G
  hgvsp: ENST00000414202.2:c.2496A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6533
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2700
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu832Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

9-5763524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763524
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763524
    reference: chr 9
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.128C>T
  hgvsp: ENSP00000442632.1:p.Arg44Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2497C>T
  hgvsp: ENSP00000251879.6:p.Arg833Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2149C>T
  hgvsp: ENSP00000398823.2:p.Arg717Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2260C>T
  hgvsp: ENSP00000370943.2:p.Arg754Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2171C>T
  hgvsp: ENSP00000439488.1:p.Arg725Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2260C>T
  hgvsp: ENSP00000402240.3:p.Arg754Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2497C>T
  hgvsp: ENSP00000416696.2:p.Arg833Cys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3196C>T
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg833Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

9-5763525-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763525
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763525
    reference: chr 9
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2261G>A
  hgvsp: ENSP00000402240.3:p.Arg754His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2261G>A
  hgvsp: ENSP00000370943.2:p.Arg754His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.129G>A
  hgvsp: ENSP00000442632.1:p.Arg44His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2172G>A
  hgvsp: ENSP00000439488.1:p.Arg725His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3197G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2498G>A
  hgvsp: ENSP00000416696.2:p.Arg833His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2150G>A
  hgvsp: ENSP00000398823.2:p.Arg717His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2498G>A
  hgvsp: ENSP00000251879.6:p.Arg833His
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3589
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg833His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

9-5763526-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763526
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763526
    reference: chr 9
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2262T>G
  hgvsp: ENST00000418622.3:c.2262T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3198T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2262T>G
  hgvsp: ENST00000381532.2:c.2262T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.130T>G
  hgvsp: ENST00000545243.1:c.130T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2151T>G
  hgvsp: ENST00000449720.2:c.2151T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2499T>G
  hgvsp: ENST00000251879.6:c.2499T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2173T>G
  hgvsp: ENST00000545641.1:c.2173T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2499T>G
  hgvsp: ENST00000414202.2:c.2499T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg833Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS

9-5763530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763530
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763530
    reference: chr 9
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2266C>T
  hgvsp: ENSP00000370943.2:p.Leu756Phe
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3202C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2177C>T
  hgvsp: ENSP00000439488.1:p.Leu727Phe
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2503C>T
  hgvsp: ENSP00000416696.2:p.Leu835Phe
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.134C>T
  hgvsp: ENSP00000442632.1:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2266C>T
  hgvsp: ENSP00000402240.3:p.Leu756Phe
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2155C>T
  hgvsp: ENSP00000398823.2:p.Leu719Phe
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2503C>T
  hgvsp: ENSP00000251879.6:p.Leu835Phe
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14827
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6529
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu835Phe
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

9-5763536-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763536
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763536
    reference: chr 9
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3208G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2272G>C
  hgvsp: ENSP00000402240.3:p.Val758Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2509G>C
  hgvsp: ENSP00000251879.6:p.Val837Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2272G>C
  hgvsp: ENSP00000370943.2:p.Val758Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2161G>C
  hgvsp: ENSP00000398823.2:p.Val721Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2183G>C
  hgvsp: ENSP00000439488.1:p.Val729Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.140G>C
  hgvsp: ENSP00000442632.1:p.Val48Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2509G>C
  hgvsp: ENSP00000416696.2:p.Val837Leu
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val837Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS

9-5763538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763538
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763538
    reference: chr 9
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2185C>T
  hgvsp: ENST00000545641.1:c.2185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2163C>T
  hgvsp: ENST00000449720.2:c.2163C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2274C>T
  hgvsp: ENST00000418622.3:c.2274C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3210C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.142C>T
  hgvsp: ENST00000545243.1:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2511C>T
  hgvsp: ENST00000251879.6:c.2511C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2274C>T
  hgvsp: ENST00000381532.2:c.2274C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2511C>T
  hgvsp: ENST00000414202.2:c.2511C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4919
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3581
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val837Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

9-5763544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763544
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763544
    reference: chr 9
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3216C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2280C>T
  hgvsp: ENST00000418622.3:c.2280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2517C>T
  hgvsp: ENST00000414202.2:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2169C>T
  hgvsp: ENST00000449720.2:c.2169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2280C>T
  hgvsp: ENST00000381532.2:c.2280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2191C>T
  hgvsp: ENST00000545641.1:c.2191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.148C>T
  hgvsp: ENST00000545243.1:c.148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2517C>T
  hgvsp: ENST00000251879.6:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17732
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2699
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn839Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

9-5763547-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763547
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763547
    reference: chr 9
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.151T>C
  hgvsp: ENST00000545243.1:c.151T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2283T>C
  hgvsp: ENST00000381532.2:c.2283T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2172T>C
  hgvsp: ENST00000449720.2:c.2172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3219T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2194T>C
  hgvsp: ENST00000545641.1:c.2194T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2520T>C
  hgvsp: ENST00000251879.6:c.2520T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2283T>C
  hgvsp: ENST00000418622.3:c.2283T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2520T>C
  hgvsp: ENST00000414202.2:c.2520T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6533
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu840Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

9-5763560-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763560
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763560
    reference: chr 9
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2296T>C
  hgvsp: ENST00000418622.3:c.2296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3232T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.164T>C
  hgvsp: ENST00000545243.1:c.164T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2185T>C
  hgvsp: ENST00000449720.2:c.2185T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2533T>C
  hgvsp: ENST00000414202.2:c.2533T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2296T>C
  hgvsp: ENST00000381532.2:c.2296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2207T>C
  hgvsp: ENST00000545641.1:c.2207T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2533T>C
  hgvsp: ENST00000251879.6:c.2533T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4920
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu845Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

9-5763577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763577
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763577
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2550C>T
  hgvsp: ENST00000414202.2:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2224C>T
  hgvsp: ENST00000545641.1:c.2224C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2313C>T
  hgvsp: ENST00000381532.2:c.2313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3249C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.181C>T
  hgvsp: ENST00000545243.1:c.181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2550C>T
  hgvsp: ENST00000251879.6:c.2550C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2202C>T
  hgvsp: ENST00000449720.2:c.2202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2313C>T
  hgvsp: ENST00000418622.3:c.2313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser850Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

9-5763578-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763578
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763578
    reference: chr 9
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2551T>G
  hgvsp: ENSP00000251879.6:p.Cys851Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2203T>G
  hgvsp: ENSP00000398823.2:p.Cys735Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.182T>G
  hgvsp: ENSP00000442632.1:p.Cys62Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2314T>G
  hgvsp: ENSP00000370943.2:p.Cys772Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2551T>G
  hgvsp: ENSP00000416696.2:p.Cys851Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2225T>G
  hgvsp: ENSP00000439488.1:p.Cys743Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2314T>G
  hgvsp: ENSP00000402240.3:p.Cys772Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3250T>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys851Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

9-5763586-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763586
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763586
    reference: chr 9
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2559A>G
  hgvsp: ENST00000251879.6:c.2559A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2559A>G
  hgvsp: ENST00000414202.2:c.2559A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2322A>G
  hgvsp: ENST00000418622.3:c.2322A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2211A>G
  hgvsp: ENST00000449720.2:c.2211A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.190A>G
  hgvsp: ENST00000545243.1:c.190A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2322A>G
  hgvsp: ENST00000381532.2:c.2322A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3258A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2233A>G
  hgvsp: ENST00000545641.1:c.2233A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2700
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr853Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

9-5763587-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763587
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763587
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2560T>C
  hgvsp: ENST00000251879.6:c.2560T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2323T>C
  hgvsp: ENST00000381532.2:c.2323T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2560T>C
  hgvsp: ENST00000414202.2:c.2560T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2234T>C
  hgvsp: ENST00000545641.1:c.2234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.191T>C
  hgvsp: ENST00000545243.1:c.191T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2323T>C
  hgvsp: ENST00000418622.3:c.2323T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2212T>C
  hgvsp: ENST00000449720.2:c.2212T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3259T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15957
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6539
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4922
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu854Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

9-5763610-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763610
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763610
    reference: chr 9
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2583G>C
  hgvsp: ENST00000251879.6:c.2583G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2346G>C
  hgvsp: ENST00000418622.3:c.2346G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2257G>C
  hgvsp: ENST00000545641.1:c.2257G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2346G>C
  hgvsp: ENST00000381532.2:c.2346G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.214G>C
  hgvsp: ENST00000545243.1:c.214G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2583G>C
  hgvsp: ENST00000414202.2:c.2583G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2235G>C
  hgvsp: ENST00000449720.2:c.2235G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3282G>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2700
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu861Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-5763616-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763616
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763616
    reference: chr 9
allele count: 43
allele frequency: 3.542593507991432e-4
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3288C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2352C>T
  hgvsp: ENST00000381532.2:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2241C>T
  hgvsp: ENST00000449720.2:c.2241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.220C>T
  hgvsp: ENST00000545243.1:c.220C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2352C>T
  hgvsp: ENST00000418622.3:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2589C>T
  hgvsp: ENST00000414202.2:c.2589C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2589C>T
  hgvsp: ENST00000251879.6:c.2589C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2263C>T
  hgvsp: ENST00000545641.1:c.2263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17757
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6541
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu863Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-5763642-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763642
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763642
    reference: chr 9
allele count: 7
allele frequency: 5.766632616074076e-5
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2289A>C
  hgvsp: ENSP00000439488.1:p.Glu764Ala
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3314A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2615A>C
  hgvsp: ENSP00000251879.6:p.Glu872Ala
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.246A>C
  hgvsp: ENSP00000442632.1:p.Glu83Ala
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2267A>C
  hgvsp: ENSP00000398823.2:p.Glu756Ala
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2378A>C
  hgvsp: ENSP00000402240.3:p.Glu793Ala
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2615A>C
  hgvsp: ENSP00000416696.2:p.Glu872Ala
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2378A>C
  hgvsp: ENSP00000370943.2:p.Glu793Ala
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4921
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu872Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

9-5763653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763653
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763653
    reference: chr 9
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2278C>T
  hgvsp: ENSP00000398823.2:p.Arg760Trp
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2300C>T
  hgvsp: ENSP00000439488.1:p.Arg768Trp
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2389C>T
  hgvsp: ENSP00000370943.2:p.Arg797Trp
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3325C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2626C>T
  hgvsp: ENSP00000416696.2:p.Arg876Trp
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2389C>T
  hgvsp: ENSP00000402240.3:p.Arg797Trp
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.257C>T
  hgvsp: ENSP00000442632.1:p.Arg87Trp
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2626C>T
  hgvsp: ENSP00000251879.6:p.Arg876Trp
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15966
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg876Trp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/9-5763653-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763653
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763653
    reference: chr 9
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3325C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2389C>A
  hgvsp: ENST00000381532.2:c.2389C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2389C>A
  hgvsp: ENST00000418622.3:c.2389C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.257C>A
  hgvsp: ENST00000545243.1:c.257C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2626C>A
  hgvsp: ENST00000251879.6:c.2626C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2626C>A
  hgvsp: ENST00000414202.2:c.2626C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2278C>A
  hgvsp: ENST00000449720.2:c.2278C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2300C>A
  hgvsp: ENST00000545641.1:c.2300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg876Arg
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

9-5763654-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763654
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763654
    reference: chr 9
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2390G>A
  hgvsp: ENSP00000402240.3:p.Arg797Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2301G>A
  hgvsp: ENSP00000439488.1:p.Arg768Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3326G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2390G>A
  hgvsp: ENSP00000370943.2:p.Arg797Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.258G>A
  hgvsp: ENSP00000442632.1:p.Arg87Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2627G>A
  hgvsp: ENSP00000251879.6:p.Arg876Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2627G>A
  hgvsp: ENSP00000416696.2:p.Arg876Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2279G>A
  hgvsp: ENSP00000398823.2:p.Arg760Gln
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17736
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg876Gln
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

9-5763657-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763657
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763657
    reference: chr 9
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.261A>G
  hgvsp: ENSP00000442632.1:p.Glu88Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2393A>G
  hgvsp: ENSP00000370943.2:p.Glu798Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2630A>G
  hgvsp: ENSP00000416696.2:p.Glu877Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3329A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2282A>G
  hgvsp: ENSP00000398823.2:p.Glu761Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2304A>G
  hgvsp: ENSP00000439488.1:p.Glu769Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2630A>G
  hgvsp: ENSP00000251879.6:p.Glu877Gly
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2393A>G
  hgvsp: ENSP00000402240.3:p.Glu798Gly
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4920
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu877Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-5763667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763667
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763667
    reference: chr 9
allele count: 9
allele frequency: 7.41485277397881e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2292C>T
  hgvsp: ENST00000449720.2:c.2292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3339C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2640C>T
  hgvsp: ENST00000414202.2:c.2640C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2403C>T
  hgvsp: ENST00000418622.3:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2314C>T
  hgvsp: ENST00000545641.1:c.2314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.271C>T
  hgvsp: ENST00000545243.1:c.271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2640C>T
  hgvsp: ENST00000251879.6:c.2640C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2403C>T
  hgvsp: ENST00000381532.2:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro880Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

9-5763681-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763681
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763681
    reference: chr 9
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2417C>T
  hgvsp: ENSP00000370943.2:p.Pro806Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2654C>T
  hgvsp: ENSP00000416696.2:p.Pro885Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3353C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2417C>T
  hgvsp: ENSP00000402240.3:p.Pro806Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2328C>T
  hgvsp: ENSP00000439488.1:p.Pro777Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2654C>T
  hgvsp: ENSP00000251879.6:p.Pro885Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.285C>T
  hgvsp: ENSP00000442632.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2306C>T
  hgvsp: ENSP00000398823.2:p.Pro769Leu
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6553
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro885Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

9-5763690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763690
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763690
    reference: chr 9
allele count: 6
allele frequency: 4.943398091848337e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2663C>T
  hgvsp: ENSP00000251879.6:p.Ala888Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2315C>T
  hgvsp: ENSP00000398823.2:p.Ala772Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2337C>T
  hgvsp: ENSP00000439488.1:p.Ala780Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.294C>T
  hgvsp: ENSP00000442632.1:p.Ala99Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2663C>T
  hgvsp: ENSP00000416696.2:p.Ala888Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2426C>T
  hgvsp: ENSP00000402240.3:p.Ala809Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2426C>T
  hgvsp: ENSP00000370943.2:p.Ala809Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3362C>T
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala888Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

9-5763692-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763692
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763692
    reference: chr 9
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2317A>G
  hgvsp: ENSP00000398823.2:p.Lys773Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2665A>G
  hgvsp: ENSP00000251879.6:p.Lys889Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2339A>G
  hgvsp: ENSP00000439488.1:p.Lys781Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2665A>G
  hgvsp: ENSP00000416696.2:p.Lys889Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2428A>G
  hgvsp: ENSP00000402240.3:p.Lys810Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2428A>G
  hgvsp: ENSP00000370943.2:p.Lys810Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.296A>G
  hgvsp: ENSP00000442632.1:p.Lys100Glu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3364A>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4915
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15987
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys889Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

9-5763712-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763712
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763712
    reference: chr 9
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2337C>G
  hgvsp: ENST00000449720.2:c.2337C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3384C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2448C>G
  hgvsp: ENST00000381532.2:c.2448C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2685C>G
  hgvsp: ENST00000251879.6:c.2685C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2685C>G
  hgvsp: ENST00000414202.2:c.2685C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.316C>G
  hgvsp: ENST00000545243.1:c.316C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2359C>G
  hgvsp: ENST00000545641.1:c.2359C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2448C>G
  hgvsp: ENST00000418622.3:c.2448C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17756
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5343
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro895Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-5763719-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763719
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763719
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2692C>G
  hgvsp: ENSP00000416696.2:p.Leu898Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2455C>G
  hgvsp: ENSP00000402240.3:p.Leu819Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2455C>G
  hgvsp: ENSP00000370943.2:p.Leu819Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.323C>G
  hgvsp: ENSP00000442632.1:p.Leu109Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2366C>G
  hgvsp: ENSP00000439488.1:p.Leu790Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3391C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2344C>G
  hgvsp: ENSP00000398823.2:p.Leu782Val
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2692C>G
  hgvsp: ENSP00000251879.6:p.Leu898Val
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3814
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu898Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

9-5763727-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763727
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763727
    reference: chr 9
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2463A>T
  hgvsp: ENST00000381532.2:c.2463A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2352A>T
  hgvsp: ENST00000449720.2:c.2352A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2463A>T
  hgvsp: ENST00000418622.3:c.2463A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2700A>T
  hgvsp: ENST00000251879.6:c.2700A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.331A>T
  hgvsp: ENST00000545243.1:c.331A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2374A>T
  hgvsp: ENST00000545641.1:c.2374A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2700A>T
  hgvsp: ENST00000414202.2:c.2700A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3399A>T
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr900Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

9-5763728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763728
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763728
    reference: chr 9
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2701G>A
  hgvsp: ENSP00000251879.6:p.Val901Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2464G>A
  hgvsp: ENSP00000370943.2:p.Val822Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.332G>A
  hgvsp: ENSP00000442632.1:p.Val112Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2464G>A
  hgvsp: ENSP00000402240.3:p.Val822Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3400G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2353G>A
  hgvsp: ENSP00000398823.2:p.Val785Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2375G>A
  hgvsp: ENSP00000439488.1:p.Val793Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2701G>A
  hgvsp: ENSP00000416696.2:p.Val901Ile
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15990
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val901Ile
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

9-5763733-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763733
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763733
    reference: chr 9
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2469C>G
  hgvsp: ENST00000418622.3:c.2469C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2706C>G
  hgvsp: ENST00000414202.2:c.2706C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2380C>G
  hgvsp: ENST00000545641.1:c.2380C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2706C>G
  hgvsp: ENST00000251879.6:c.2706C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2358C>G
  hgvsp: ENST00000449720.2:c.2358C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.337C>G
  hgvsp: ENST00000545243.1:c.337C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2469C>G
  hgvsp: ENST00000381532.2:c.2469C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3405C>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14882
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val902Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

9-5763744-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763744
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763744
    reference: chr 9
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2717G>T
  hgvsp: ENSP00000251879.6:p.Arg906Met
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2391G>T
  hgvsp: ENSP00000439488.1:p.Arg798Met
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3416G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2369G>T
  hgvsp: ENSP00000398823.2:p.Arg790Met
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2480G>T
  hgvsp: ENSP00000370943.2:p.Arg827Met
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2480G>T
  hgvsp: ENSP00000402240.3:p.Arg827Met
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.348G>T
  hgvsp: ENSP00000442632.1:p.Arg117Met
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2717G>T
  hgvsp: ENSP00000416696.2:p.Arg906Met
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4920
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15990
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg906Met
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

9-5763751-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763751
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763751
    reference: chr 9
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2724C>T
  hgvsp: ENST00000251879.6:c.2724C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2487C>T
  hgvsp: ENST00000418622.3:c.2487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2398C>T
  hgvsp: ENST00000545641.1:c.2398C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2376C>T
  hgvsp: ENST00000449720.2:c.2376C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2487C>T
  hgvsp: ENST00000381532.2:c.2487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2724C>T
  hgvsp: ENST00000414202.2:c.2724C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.355C>T
  hgvsp: ENST00000545243.1:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3423C>T
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr908Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

9-5763757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763757
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763757
    reference: chr 9
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2730T>C
  hgvsp: ENST00000251879.6:c.2730T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2493T>C
  hgvsp: ENST00000381532.2:c.2493T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.361T>C
  hgvsp: ENST00000545243.1:c.361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2730T>C
  hgvsp: ENST00000414202.2:c.2730T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2404T>C
  hgvsp: ENST00000545641.1:c.2404T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2382T>C
  hgvsp: ENST00000449720.2:c.2382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2493T>C
  hgvsp: ENST00000418622.3:c.2493T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3429T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr910Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

9-5763762-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763762
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763762
    reference: chr 9
allele count: 3
allele frequency: 2.473696362017217e-5
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2387T>G
  hgvsp: ENSP00000398823.2:p.Leu796Arg
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2498T>G
  hgvsp: ENSP00000402240.3:p.Leu833Arg
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.366T>G
  hgvsp: ENSP00000442632.1:p.Leu123Arg
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2409T>G
  hgvsp: ENSP00000439488.1:p.Leu804Arg
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2735T>G
  hgvsp: ENSP00000251879.6:p.Leu912Arg
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2498T>G
  hgvsp: ENSP00000370943.2:p.Leu833Arg
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3434T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2735T>G
  hgvsp: ENSP00000416696.2:p.Leu912Arg
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15991
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu912Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-5763785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763785
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763785
    reference: chr 9
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2432G>A
  hgvsp: ENSP00000439488.1:p.Val812Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2410G>A
  hgvsp: ENSP00000398823.2:p.Val804Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2521G>A
  hgvsp: ENSP00000402240.3:p.Val841Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2521G>A
  hgvsp: ENSP00000370943.2:p.Val841Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3457G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2758G>A
  hgvsp: ENSP00000251879.6:p.Val920Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.389G>A
  hgvsp: ENSP00000442632.1:p.Val131Ile
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2758G>A
  hgvsp: ENSP00000416696.2:p.Val920Ile
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17376
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val920Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

9-5763800-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763800
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763800
    reference: chr 9
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2536G>C
  hgvsp: ENSP00000370943.2:p.Asp846His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2447G>C
  hgvsp: ENSP00000439488.1:p.Asp817His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2773G>C
  hgvsp: ENSP00000251879.6:p.Asp925His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2773G>C
  hgvsp: ENSP00000416696.2:p.Asp925His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2425G>C
  hgvsp: ENSP00000398823.2:p.Asp809His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.404G>C
  hgvsp: ENSP00000442632.1:p.Asp136His
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3472G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2536G>C
  hgvsp: ENSP00000402240.3:p.Asp846His
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15988
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp925His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

9-5763807-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763807
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763807
    reference: chr 9
allele count: 1
allele frequency: 8.304130474498016e-6
allele num: 120422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3479T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2543T>C
  hgvsp: ENSP00000402240.3:p.Phe848Ser
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2454T>C
  hgvsp: ENSP00000439488.1:p.Phe819Ser
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2543T>C
  hgvsp: ENSP00000370943.2:p.Phe848Ser
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.411T>C
  hgvsp: ENSP00000442632.1:p.Phe138Ser
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2780T>C
  hgvsp: ENSP00000251879.6:p.Phe927Ser
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2432T>C
  hgvsp: ENSP00000398823.2:p.Phe811Ser
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2780T>C
  hgvsp: ENSP00000416696.2:p.Phe927Ser
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4908
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6355
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe927Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

9-5763811-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763811
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763811
    reference: chr 9
allele count: 15
allele frequency: 1.24630263551464e-4
allele num: 120356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3483G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2436G>A
  hgvsp: ENST00000449720.2:c.2436G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.415G>A
  hgvsp: ENST00000545243.1:c.415G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2784G>A
  hgvsp: ENST00000251879.6:c.2784G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2784G>A
  hgvsp: ENST00000414202.2:c.2784G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2547G>A
  hgvsp: ENST00000381532.2:c.2547G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2458G>A
  hgvsp: ENST00000545641.1:c.2458G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2547G>A
  hgvsp: ENST00000418622.3:c.2547G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11930
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3520
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu928Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

9-5763812-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763812
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763812
    reference: chr 9
allele count: 1
allele frequency: 8.310617645103384e-6
allele num: 120328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2548G>A
  hgvsp: ENSP00000370943.2:p.Glu850Lys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2548G>A
  hgvsp: ENSP00000402240.3:p.Glu850Lys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3484G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2459G>A
  hgvsp: ENSP00000439488.1:p.Glu821Lys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.416G>A
  hgvsp: ENSP00000442632.1:p.Glu140Lys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2437G>A
  hgvsp: ENSP00000398823.2:p.Glu813Lys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2785G>A
  hgvsp: ENSP00000416696.2:p.Glu929Lys
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2785G>A
  hgvsp: ENSP00000251879.6:p.Glu929Lys
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4904
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6336
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu929Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

9-5763812-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763812
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763812
    reference: chr 9
allele count: 1
allele frequency: 8.310617645103384e-6
allele num: 120328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2459G>C
  hgvsp: ENSP00000439488.1:p.Glu821Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2548G>C
  hgvsp: ENSP00000402240.3:p.Glu850Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2785G>C
  hgvsp: ENSP00000251879.6:p.Glu929Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2548G>C
  hgvsp: ENSP00000370943.2:p.Glu850Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2785G>C
  hgvsp: ENSP00000416696.2:p.Glu929Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.416G>C
  hgvsp: ENSP00000442632.1:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3484G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2437G>C
  hgvsp: ENSP00000398823.2:p.Glu813Gln
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu929Gln
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

9-5763838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763838
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763838
    reference: chr 9
allele count: 1
allele frequency: 8.398138972403716e-6
allele num: 119074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3510C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2811C>T
  hgvsp: ENST00000414202.2:c.2811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2574C>T
  hgvsp: ENST00000418622.3:c.2574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2574C>T
  hgvsp: ENST00000381532.2:c.2574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.442C>T
  hgvsp: ENST00000545243.1:c.442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2463C>T
  hgvsp: ENST00000449720.2:c.2463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2485C>T
  hgvsp: ENST00000545641.1:c.2485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2811C>T
  hgvsp: ENST00000251879.6:c.2811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5285
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4895
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp937Asp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

9-5763858-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763858
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763858
    reference: chr 9
allele count: 1
allele frequency: 8.606148232297153e-6
allele num: 116196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.462T>C
  hgvsp: ENSP00000442632.1:p.Ile155Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2594T>C
  hgvsp: ENSP00000402240.3:p.Ile865Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3530T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2483T>C
  hgvsp: ENSP00000398823.2:p.Ile828Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2831T>C
  hgvsp: ENSP00000251879.6:p.Ile944Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2831T>C
  hgvsp: ENSP00000416696.2:p.Ile944Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2594T>C
  hgvsp: ENSP00000370943.2:p.Ile865Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2505T>C
  hgvsp: ENSP00000439488.1:p.Ile836Thr
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15987
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile944Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

9-5763871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763871
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763871
    reference: chr 9
allele count: 8
allele frequency: 6.979828296223913e-5
allele num: 114616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+3A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+3A>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12723
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5870
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3941
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2841+3A>G
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/9-5763873-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763873
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763873
    reference: chr 9
allele count: 3831
allele frequency: 3.354347255056475e-2
allele num: 114210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+5C>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+5C>A
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 7.5e0
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 6.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 1.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 11200
  bin: 2.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 9.75e1
  variant carriers: 2427
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 3.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4560
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11150
  bin: 6.25e1
  variant carriers: 3
hgvs: c.2841+5C>A
num of homozygotes: 92
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

9-5763875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763875
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763875
    reference: chr 9
allele count: 1
allele frequency: 8.772391529378739e-6
allele num: 113994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+7A>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+7A>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2841+7A>G
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

9-5763878-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763878
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763878
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 113576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+10C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+10C>T
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17177
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

9-5763881-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763881
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763881
    reference: chr 9
allele count: 1
allele frequency: 8.826436943934473e-6
allele num: 113296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+13T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+13T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3754
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10898
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5059
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

9-5763887-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763887
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763887
    reference: chr 9
allele count: 1
allele frequency: 8.876580031245562e-6
allele num: 112656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+19T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+19T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17178
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-5763889-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763889
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763889
    reference: chr 9
allele count: 1
allele frequency: 8.896005693443644e-6
allele num: 112410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+21A>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+21A>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10453
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

9-5763891-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763891
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763891
    reference: chr 9
allele count: 2
allele frequency: 1.779771121433784e-5
allele num: 112374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+23G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+23G>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

9-5763895-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763895
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763895
    reference: chr 9
allele count: 1
allele frequency: 8.95078856447253e-6
allele num: 111722
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+27C>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+27C>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3755
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

9-5763901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763901
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763901
    reference: chr 9
allele count: 1
allele frequency: 9.056494412142948e-6
allele num: 110418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+33T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+33T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9987
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

9-5763902-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763902
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763902
    reference: chr 9
allele count: 1
allele frequency: 9.056330374932077e-6
allele num: 110420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+34T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+34T>G
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2058
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3755
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

9-5763908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763908
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763908
    reference: chr 9
allele count: 7
allele frequency: 6.384065372829418e-5
allele num: 109648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+40G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+40G>A
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7309
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10901
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

9-5763911-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763911
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763912
    reference: chr 9
allele count: 2
allele frequency: 1.833516685001834e-5
allele num: 109080
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+46dupA
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+46dupA
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3754
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2218
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-5763917-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5763917
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5763917
    reference: chr 9
allele count: 1
allele frequency: 9.287293125545628e-6
allele num: 107674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2604+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2841+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3540+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2515+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2841+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2604+49T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2493+49T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5358
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

9-5765363-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765363
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765363
    reference: chr 9
allele count: 1
allele frequency: 8.617272460920669e-6
allele num: 116046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-51T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-51T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-51T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1495T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-51T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-51T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*509A>G
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-51T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-51T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-5765375-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765375
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765374
    reference: chr 9
allele count: 1
allele frequency: 8.602002546192754e-6
allele num: 116252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*496delA
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-38delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-38delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1508delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-38delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-38delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-38delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-38delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-38delT
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3652
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GT
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

9-5765376-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765376
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765376
    reference: chr 9
allele count: 4
allele frequency: 3.44050506614371e-5
allele num: 116262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-38T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-38T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-38T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-38T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-38T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*496A>G
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-38T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1508T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-38T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31043
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

9-5765378-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765378
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765378
    reference: chr 9
allele count: 1
allele frequency: 8.599339570720968e-6
allele num: 116288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-36G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1510G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-36G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-36G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-36G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*494C>A
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-36G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-36G>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-36G>T
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3568
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

9-5765381-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765381
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765381
    reference: chr 9
allele count: 798
allele frequency: 6.854139109820831e-3
allele num: 116426
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-33T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1513T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*491A>C
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-33T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-33T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-33T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-33T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-33T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-33T>G
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 6.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 8.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 5.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 5.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 6.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 9.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7156
  bin: 4.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 3.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 4.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3623
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 32
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

9-5765400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765400
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765400
    reference: chr 9
allele count: 1
allele frequency: 8.472565831836514e-6
allele num: 118028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-14G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-14G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*472C>T
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-14G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-14G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-14G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-14G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1532G>A
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-14G>A
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30995
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

9-5765402-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765402
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765402
    reference: chr 9
allele count: 12
allele frequency: 1.01490214651804e-4
allele num: 118238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-12T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-12T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1534T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-12T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-12T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*470A>C
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-12T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-12T>G
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-12T>G
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7734
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

9-5765403-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765403
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765402
    reference: chr 9
allele count: 1
allele frequency: 8.451513666097598e-6
allele num: 118322
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-5delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-5delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-5delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1541delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-5delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-5delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*468delA
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-5delT
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-5delT
  variant of: http://identifiers.org/hgnc/17686
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: GT
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-5765408-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765408
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765408
    reference: chr 9
allele count: 10
allele frequency: 8.420910805712746e-5
allele num: 118752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2842-6T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1540T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2605-6T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2842-6T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2494-6T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2516-6T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2605-6T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*464A>G
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3541-6T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2842-6T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

9-5765418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765418
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765418
    reference: chr 9
allele count: 1
allele frequency: 8.355475342992263e-6
allele num: 119682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3545T>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2846T>C
  hgvsp: ENSP00000251879.6:p.Met949Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2846T>C
  hgvsp: ENSP00000416696.2:p.Met949Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2609T>C
  hgvsp: ENSP00000402240.3:p.Met870Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2498T>C
  hgvsp: ENSP00000398823.2:p.Met833Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2520T>C
  hgvsp: ENSP00000439488.1:p.Met841Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2609T>C
  hgvsp: ENSP00000370943.2:p.Met870Thr
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*454A>G
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1550T>C
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met949Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

9-5765423-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765423
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765423
    reference: chr 9
allele count: 4
allele frequency: 3.330835206928137e-5
allele num: 120090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1555G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2503G>C
  hgvsp: ENSP00000398823.2:p.Val835Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2851G>C
  hgvsp: ENSP00000416696.2:p.Val951Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2525G>C
  hgvsp: ENSP00000439488.1:p.Val843Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2614G>C
  hgvsp: ENSP00000402240.3:p.Val872Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2614G>C
  hgvsp: ENSP00000370943.2:p.Val872Leu
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*449C>G
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3550G>C
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2851G>C
  hgvsp: ENSP00000251879.6:p.Val951Leu
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val951Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-5765425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5765425
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 5765425
    reference: chr 9
allele count: 1
allele frequency: 8.316561600771776e-6
allele num: 120242
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000416696
  ensembl transcript: ENST00000414202
  gene symbol: KIAA1432
  hgvsc: ENST00000414202.2:c.2853C>T
  hgvsp: ENST00000414202.2:c.2853C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000251879
  ensembl transcript: ENST00000251879
  gene symbol: KIAA1432
  hgvsc: ENST00000251879.6:c.2853C>T
  hgvsp: ENST00000251879.6:c.2853C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000442632
  ensembl transcript: ENST00000545243
  gene symbol: KIAA1432
  hgvsc: ENST00000545243.1:c.472+1557C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099219
  ensembl protein: ENSP00000417160
  ensembl transcript: ENST00000462592
  gene symbol: ERMP1
  hgvsc: ENST00000462592.1:c.*447G>A
  variant of: http://identifiers.org/hgnc/23703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107036
  ensembl transcript: ENST00000276898
  gene symbol: KIAA1432
  hgvsc: ENST00000276898.3:n.3552C>T
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000439488
  ensembl transcript: ENST00000545641
  gene symbol: KIAA1432
  hgvsc: ENST00000545641.1:c.2527C>T
  hgvsp: ENST00000545641.1:c.2527C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000398823
  ensembl transcript: ENST00000449720
  gene symbol: KIAA1432
  hgvsc: ENST00000449720.2:c.2505C>T
  hgvsp: ENST00000449720.2:c.2505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000370943
  ensembl transcript: ENST00000381532
  gene symbol: KIAA1432
  hgvsc: ENST00000381532.2:c.2616C>T
  hgvsp: ENST00000381532.2:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107036
  ensembl protein: ENSP00000402240
  ensembl transcript: ENST00000418622
  gene symbol: KIAA1432
  hgvsc: ENST00000418622.3:c.2616C>T
  hgvsp: ENST00000418622.3:c.2616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17686
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val951Val
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 2700
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4919
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17743
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6525
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.349e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.985479e6

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.257e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5359
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4917
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2701
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.691e1

VQSLOD
type: SiteQuality
SIO_000300: -3.331e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.667e0

FS
type: SiteQuality
SIO_000300: 5.719e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.985417e6

GenotypeQuality
all individuals: 2701
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15941
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

QD
type: SiteQuality
SIO_000300: 9.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.242e0

FS
type: SiteQuality
SIO_000300: 1.348e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.039e0

DP
type: SiteQuality
SIO_000300: 1.985411e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

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

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

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

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15943
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5360
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
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SIO_000300: 6.19e0

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

DP
type: SiteQuality
SIO_000300: 1.985581e6

QD
type: SiteQuality
SIO_000300: 9.49e0

GenotypeQuality
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bin: 8.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.478e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 1.985536e6

GenotypeQuality
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bin: 9.25e1
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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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: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.985583e6

FS
type: SiteQuality
SIO_000300: 1.112e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.561e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: -3.253e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.56e-1

DP
type: SiteQuality
SIO_000300: 1.985621e6

VQSLOD
type: SiteQuality
SIO_000300: 4.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.594e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-2

FS
type: SiteQuality
SIO_000300: 3.359e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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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variant carriers: 1

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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.337e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.045e0

DP
type: SiteQuality
SIO_000300: 1.985618e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.0721e1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.01e-1

QD
type: SiteQuality
SIO_000300: 1.704e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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
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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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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.985887e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.658e1

FS
type: SiteQuality
SIO_000300: 3.357e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 3

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

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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bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.478664192949907e-4
allele num: 8624
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

FS
type: SiteQuality
SIO_000300: 2.15e0

MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
type: SiteQuality
SIO_000300: 1.986042e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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VQSLOD
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SIO_000300: -2.814e-1

QD
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SIO_000300: 1.483e1

ReadPosRankSum
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SIO_000300: 5.3e-1

MQRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
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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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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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QD
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.986936e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.986e0

VQSLOD
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SIO_000300: 2.75e-1

DP
type: SiteQuality
SIO_000300: 1.987068e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.059e1

BaseQRankSum
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SIO_000300: 2.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: -4.52e-1

BaseQRankSum
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 3.317e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.924e0

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

DP
type: SiteQuality
SIO_000300: 1.98728e6

MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e-1

ReadPosRankSum
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SIO_000300: -7.68e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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
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num of homozygotes: 0

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

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

Other
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.987335e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

Other
type: Population
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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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East Asian
type: Population
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allele frequency: 0.0e0
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African
type: Population
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allele frequency: 3.940034595425716e-3
allele num: 10406
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.17e-1

ReadPosRankSum
type: SiteQuality
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QD
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VQSLOD
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49265719594797e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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Other
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South Asian
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BaseQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

East Asian
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African
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Latino
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South Asian
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European (Finnish)
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MQ
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.369e1

DP
type: SiteQuality
SIO_000300: 1.989078e6

GenotypeQuality
all individuals: 15966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
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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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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3816
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

DP
type: SiteQuality
SIO_000300: 1.989078e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

FS
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.369e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

FS
type: SiteQuality
SIO_000300: 2.695e0

QD
type: SiteQuality
SIO_000300: 1.526e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 1.989169e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.0e-2

FS
type: SiteQuality
SIO_000300: 1.487e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.615e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.135e0

DP
type: SiteQuality
SIO_000300: 1.989113e6

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: 9

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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bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.348637875745497e-4
allele num: 66734
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 5.16e-1

DP
type: SiteQuality
SIO_000300: 1.990144e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e-1

QD
type: SiteQuality
SIO_000300: 1.538e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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bin: 3.25e1
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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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
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.989544e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.79e-1

FS
type: SiteQuality
SIO_000300: 1.178e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.92e0

VQSLOD
type: SiteQuality
SIO_000300: 6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.234e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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variant carriers: 6

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Other
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num of homozygotes: 0

BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.990048e6

QD
type: SiteQuality
SIO_000300: 1.275e1

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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
type: Population
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allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

Other
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQ
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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Other
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African
type: Population
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: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

East Asian
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InbreedingCoeff
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DP
type: SiteQuality
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FS
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QD
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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MQ
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DP
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QD
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SIO_000300: 1.113e1

ReadPosRankSum
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FS
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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MQ
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
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
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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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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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: 8626
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South 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 frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
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DP
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FS
type: SiteQuality
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BaseQRankSum
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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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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: 16512
num of homozygotes: 0

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

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

Other
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African
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.377e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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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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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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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66704
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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DP
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Latino
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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East Asian
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Other
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FS
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ClippingRankSum
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QD
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VQSLOD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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East Asian
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South Asian
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5314
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511715797430083e-5
allele num: 66150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.973149e6

QD
type: SiteQuality
SIO_000300: 1.099e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.985e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.717e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.131e0

GenotypeQuality
all individuals: 16973
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15987
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5311
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3529
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513271390091099e-5
allele num: 66082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.970619e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: -4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

QD
type: SiteQuality
SIO_000300: 1.3e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

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

GenotypeQuality
all individuals: 6341
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4905
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15999
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2689
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16924
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.096422073984233e-4
allele num: 16490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.255e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

FS
type: SiteQuality
SIO_000300: 5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 1.970372e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-1

GenotypeQuality
all individuals: 16925
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3812
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15989
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2689
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.895111814763506e-5
allele num: 10106
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66022
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

FS
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 1.96924e6

QD
type: SiteQuality
SIO_000300: 1.887e1

MQ
type: SiteQuality
SIO_000300: 5.93e1

VQSLOD
type: SiteQuality
SIO_000300: -5.776e-1

GenotypeQuality
all individuals: 4904
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3812
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15989
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2689
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514646632940535e-5
allele num: 66022
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.887e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.776e-1

FS
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.96924e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

GenotypeQuality
all individuals: 115
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15987
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6155
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65434
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16060
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.172e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.982e0

FS
type: SiteQuality
SIO_000300: 1.2643e1

VQSLOD
type: SiteQuality
SIO_000300: -2.411e0

QD
type: SiteQuality
SIO_000300: 1.034e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.950005e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5946
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13718
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4888
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558409175913228e-5
allele num: 64168
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14942
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.064e0

QD
type: SiteQuality
SIO_000300: 1.493e1

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.911986e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

GenotypeQuality
all individuals: 324
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12200
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15992
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5241
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.345794392523365e-4
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14166
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.886796e6

FS
type: SiteQuality
SIO_000300: 1.475e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

GenotypeQuality
all individuals: 4917
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2502
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3543
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3227
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 5472
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 18547
bin: 9.75e1
variant carriers: 3736

South Asian
type: Population
allele count: 108
allele frequency: 7.733066017471001e-3
allele num: 13966
num of homozygotes: 1

Latino
type: Population
allele count: 229
allele frequency: 1.989228630993746e-2
allele num: 11512
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 2962
allele frequency: 4.663098236775819e-2
allele num: 63520
num of homozygotes: 66

African
type: Population
allele count: 75
allele frequency: 8.162821070962124e-3
allele num: 9188
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

Other
type: Population
allele count: 22
allele frequency: 2.564102564102564e-2
allele num: 858
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 434
allele frequency: 6.563823351482154e-2
allele num: 6612
num of homozygotes: 19

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

FS
type: SiteQuality
SIO_000300: 6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.27e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 2.167817e6

QD
type: SiteQuality
SIO_000300: 1.27e1

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11399
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17177
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.091464745688714e-4
allele num: 9162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 7.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 7.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.947217e6

GenotypeQuality
all individuals: 5059
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4744
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3754
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.941908e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.94e0

QD
type: SiteQuality
SIO_000300: 1.115e1

GenotypeQuality
all individuals: 144
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5618
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63182
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 1.937872e6

MQ
type: SiteQuality
SIO_000300: 5.918e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

FS
type: SiteQuality
SIO_000300: 4.573e0

QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeQuality
all individuals: 3754
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3286
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62966
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.6057195010648e-5
allele num: 13148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-1

DP
type: SiteQuality
SIO_000300: 1.930508e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3754
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5056
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17177
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 570
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4440
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 2595
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variant carriers: 0

GenotypeQuality
all individuals: 4747
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.69941484447182e-5
allele num: 12988
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.92e-1

DP
type: SiteQuality
SIO_000300: 1.927901e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeQuality
all individuals: 1507
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 374
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variant carriers: 0

GenotypeQuality
all individuals: 17178
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.208480565371025e-4
allele num: 9056
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.239e0

FS
type: SiteQuality
SIO_000300: 5.736e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

DP
type: SiteQuality
SIO_000300: 1.927592e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.32e-1

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
all individuals: 2594
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62702
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.31e1

VQSLOD
type: SiteQuality
SIO_000300: -5.092e-1

FS
type: SiteQuality
SIO_000300: 1.842e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 1.923515e6

MQRankSum
type: SiteQuality
SIO_000300: -9.58e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.372e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3755
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.603489192482843e-5
allele num: 62364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 2.875e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.69e0

DP
type: SiteQuality
SIO_000300: 1.913315e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 432
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variant carriers: 0

GenotypeQuality
all individuals: 5538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 4745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.603437770580124e-5
allele num: 62366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.913091e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 3.571e0

QD
type: SiteQuality
SIO_000300: 1.248e1

GenotypeQuality
all individuals: 238
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.126561091798635e-4
allele num: 62136
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 4.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 1.908282e6

QD
type: SiteQuality
SIO_000300: 1.274e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.773e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11002
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8802
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.226951498918971e-5
allele num: 61978
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.786e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.233e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 3.71e0

DP
type: SiteQuality
SIO_000300: 1.905275e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-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

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: 778
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8714
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.624748164034575e-5
allele num: 61548
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.735e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e0

FS
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.903657e6

QD
type: SiteQuality
SIO_000300: 1.524e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13018
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.387e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.004e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

QD
type: SiteQuality
SIO_000300: 1.831e1

DP
type: SiteQuality
SIO_000300: 2.667331e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

GenotypeQuality
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bin: 4.25e1
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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GenotypeQuality
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GenotypeQuality
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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: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530737203036983e-5
allele num: 65328
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 2.236e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

DP
type: SiteQuality
SIO_000300: 2.675097e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e-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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GenotypeQuality
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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: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
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: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5916493204359e-5
allele num: 65336
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.387e1

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

FS
type: SiteQuality
SIO_000300: 1.4439e1

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
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SIO_000300: 4.96e0

DP
type: SiteQuality
SIO_000300: 2.675781e6

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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GenotypeQuality
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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: 850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65320
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.119e0

FS
type: SiteQuality
SIO_000300: 3.438e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-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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GenotypeQuality
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variant carriers: 759

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 30
allele frequency: 2.609149417289963e-3
allele num: 11498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.06063110213326e-5
allele num: 65346
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.257336343115124e-4
allele num: 13290
num of homozygotes: 0

African
type: Population
allele count: 763
allele frequency: 7.423623273010313e-2
allele num: 10278
num of homozygotes: 32

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.641e1

GenotypeQuality
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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: 13
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 1
allele frequency: 1.519987840097279e-5
allele num: 65790
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

DP
type: SiteQuality
SIO_000300: 2.710773e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 1.833e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3531
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31002
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 411
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3876
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.697439875872769e-5
allele num: 10312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.593937000698643e-5
allele num: 65842
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.337265787647467e-4
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.146788990825688e-3
allele num: 872
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

DP
type: SiteQuality
SIO_000300: 2.714142e6

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3876
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30995
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7794
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517911353976928e-5
allele num: 65880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14532
num of homozygotes: 0

Other
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: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

FS
type: SiteQuality
SIO_000300: 6.714e0

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.408e1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 2.715591e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.549e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8107
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3877
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3795
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30999
bin: 9.75e1
variant carriers: 10

South Asian
type: Population
allele count: 4
allele frequency: 2.701972439881113e-4
allele num: 14804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.936108422071636e-4
allele num: 10330
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.654410053525716e-4
allele num: 8594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65986
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

DP
type: SiteQuality
SIO_000300: 2.720821e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.581e1

GenotypeQuality
all individuals: 3850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3670
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30993
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8902
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509433962264151e-5
allele num: 66250
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

FS
type: SiteQuality
SIO_000300: 9.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 2.732847e6

MQRankSum
type: SiteQuality
SIO_000300: -9.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30993
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3879
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1959
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.026092982614722e-5
allele num: 66378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.939e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.73865e6

QD
type: SiteQuality
SIO_000300: 1.204e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.08e-1