16-15684948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15684948
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15684948
    reference: chr 16
allele count: 1
allele frequency: 9.307520476545048e-5
allele num: 10744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.334G>A
  hgvsp: ENST00000565857.1:c.334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19213
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala112Ala
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.332267519317879e-4
  allele num: 7506
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 188
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15684955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15684955
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15684955
    reference: chr 16
allele count: 1
allele frequency: 9.314456035767511e-5
allele num: 10736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.341G>A
  hgvsp: ENSP00000456084.1:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/19213
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 420
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu115Lys
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 92
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum

16-15684988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15684988
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15684988
    reference: chr 16
allele count: 1
allele frequency: 9.333582228859437e-5
allele num: 10714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+16T>C
  variant of: http://identifiers.org/hgnc/19213
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
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genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 392
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 522
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genotype quality: GenotypeQuality
  all individuals: 635
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.332622601279318e-4
  allele num: 7504
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2678
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

16-15684999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15684999
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15684999
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 10700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+27C>T
  variant of: http://identifiers.org/hgnc/19213
canonical: false
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 386
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 188
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

16-15690499-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690499
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690499
    reference: chr 16
allele count: 1
allele frequency: 8.993938085730218e-6
allele num: 111186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5527T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*534A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1903A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

16-15690503-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690503
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690503
    reference: chr 16
allele count: 1
allele frequency: 8.991835413444593e-6
allele num: 111212
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*47C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*47C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*47C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*47C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5531G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*530C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*47C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1899C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*47C>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9455
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5294
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

16-15690506-TCAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690506
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690502
    reference: chr 16
allele count: 2
allele frequency: 1.798011399392272e-5
allele num: 111234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*523_*526delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*40_*43delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1892_1895delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5538_*12+5541delACAG
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*40_*43delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*40_*43delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*40_*43delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*40_*43delTCTG
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*40_*43delTCTG
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5294
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: TCAGA
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

16-15690507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690507
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690507
    reference: chr 16
allele count: 1
allele frequency: 8.992320558243261e-6
allele num: 111206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5535C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*43G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*43G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*43G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*526G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1895G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9500
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

16-15690513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690513
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690513
    reference: chr 16
allele count: 1
allele frequency: 8.980368913554968e-6
allele num: 111354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5541G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*520C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1889C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*37C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

16-15690521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690521
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690521
    reference: chr 16
allele count: 7
allele frequency: 6.277351316450247e-5
allele num: 111512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*512G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*29G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*29G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1881G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5549C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*29G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3586
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-15690526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690526
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690526
    reference: chr 16
allele count: 6
allele frequency: 5.36346408266886e-5
allele num: 111868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*24G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*24G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1876G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*507G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5554C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22348
  bin: 9.75e1
  variant carriers: 6
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-15690534-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690534
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690534
    reference: chr 16
allele count: 1
allele frequency: 8.895214374666429e-6
allele num: 112420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*16T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*16T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5562A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*499T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*16T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*16T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*16T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*16T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1868T>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3588
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4164
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-15690534-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690534
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690534
    reference: chr 16
allele count: 1
allele frequency: 8.895214374666429e-6
allele num: 112420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*499T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*16T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5562A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*16T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*16T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1868T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*16T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*16T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*16T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

16-15690539-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690539
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690539
    reference: chr 16
allele count: 1
allele frequency: 8.86980894431534e-6
allele num: 112742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5567C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*11G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*11G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*11G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1863G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*494G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2603
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-15690542-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690542
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690542
    reference: chr 16
allele count: 3
allele frequency: 2.648305084745763e-5
allele num: 113280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*491T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*8T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*8T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5570A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*8T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*8T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*8T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*8T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1860T>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-15690542-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690542
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690542
    reference: chr 16
allele count: 1
allele frequency: 8.827683615819209e-6
allele num: 113280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*8T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*8T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*491T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5570A>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*8T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1860T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*8T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*8T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*8T>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

16-15690545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690545
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690545
    reference: chr 16
allele count: 2
allele frequency: 1.759819794453048e-5
allele num: 113648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.*5C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1857C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.*5C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.*5C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*488C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5573G>A
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

16-15690567-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690567
    reference: chr 16
allele count: 1
allele frequency: 8.511942254983741e-6
allele num: 117482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5595G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5212C>T
  hgvsp: ENSP00000379654.3:p.Pro1738Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1922C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4717C>T
  hgvsp: ENSP00000439819.2:p.Pro1573Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4276C>T
  hgvsp: ENSP00000341939.3:p.Pro1426Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5203C>T
  hgvsp: ENSP00000473601.1:p.Pro1735Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*466C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5203C>T
  hgvsp: ENSP00000449376.1:p.Pro1735Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5212C>T
  hgvsp: ENSP00000450309.1:p.Pro1738Ser
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1835C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12514
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro1738Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

16-15690571-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690571
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690571
    reference: chr 16
allele count: 1
allele frequency: 8.452942469273554e-6
allele num: 118302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*462A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5199A>T
  hgvsp: ENSP00000473601.1:p.Leu1733Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5208A>T
  hgvsp: ENSP00000379654.3:p.Leu1736Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4272A>T
  hgvsp: ENSP00000341939.3:p.Leu1424Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4713A>T
  hgvsp: ENSP00000439819.2:p.Leu1571Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5208A>T
  hgvsp: ENSP00000450309.1:p.Leu1736Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1831A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1918A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5199A>T
  hgvsp: ENSP00000449376.1:p.Leu1733Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5599T>A
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4037
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3192
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu1736Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

16-15690575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690575
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690575
    reference: chr 16
allele count: 7
allele frequency: 5.887597355627702e-5
allele num: 118894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5204C>T
  hgvsp: ENSP00000450309.1:p.Ser1735Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4268C>T
  hgvsp: ENSP00000341939.3:p.Ser1423Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4709C>T
  hgvsp: ENSP00000439819.2:p.Ser1570Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5204C>T
  hgvsp: ENSP00000379654.3:p.Ser1735Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5603G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1827C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*458C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5195C>T
  hgvsp: ENSP00000449376.1:p.Ser1732Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5195C>T
  hgvsp: ENSP00000473601.1:p.Ser1732Phe
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1914C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10470
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2608
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser1735Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/16-15690576-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690576
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690576
    reference: chr 16
allele count: 1
allele frequency: 8.402372830087217e-6
allele num: 119014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5203T>G
  hgvsp: ENSP00000450309.1:p.Ser1735Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5194T>G
  hgvsp: ENSP00000473601.1:p.Ser1732Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4708T>G
  hgvsp: ENSP00000439819.2:p.Ser1570Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1826T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4267T>G
  hgvsp: ENSP00000341939.3:p.Ser1423Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5194T>G
  hgvsp: ENSP00000449376.1:p.Ser1732Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*457T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5604A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1913T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5203T>G
  hgvsp: ENSP00000379654.3:p.Ser1735Ala
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1735Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-15690583-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690583
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690583
    reference: chr 16
allele count: 1
allele frequency: 8.356313194618534e-6
allele num: 119670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4260C>T
  hgvsp: ENST00000344181.3:c.4260C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5187C>T
  hgvsp: ENST00000548025.1:c.5187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1819C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5196C>T
  hgvsp: ENST00000396368.3:c.5196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5196C>T
  hgvsp: ENST00000551742.1:c.5196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4701C>T
  hgvsp: ENST00000540441.2:c.4701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*450C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5187C>T
  hgvsp: ENST00000602337.1:c.5187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5611G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1906C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala1732Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

16-15690591-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690591
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690591
    reference: chr 16
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5188T>C
  hgvsp: ENST00000396368.3:c.5188T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1811T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4252T>C
  hgvsp: ENST00000344181.3:c.4252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5179T>C
  hgvsp: ENST00000548025.1:c.5179T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1898T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4693T>C
  hgvsp: ENST00000540441.2:c.4693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5179T>C
  hgvsp: ENST00000602337.1:c.5179T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5188T>C
  hgvsp: ENST00000551742.1:c.5188T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5619A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*442T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu1730Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-15690615-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690615
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690615
    reference: chr 16
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1787A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5643T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5155A>G
  hgvsp: ENSP00000449376.1:p.Lys1719Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4669A>G
  hgvsp: ENSP00000439819.2:p.Lys1557Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5164A>G
  hgvsp: ENSP00000379654.3:p.Lys1722Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4228A>G
  hgvsp: ENSP00000341939.3:p.Lys1410Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1874A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*418A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5164A>G
  hgvsp: ENSP00000450309.1:p.Lys1722Glu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5155A>G
  hgvsp: ENSP00000473601.1:p.Lys1719Glu
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys1722Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

16-15690617-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690617
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690617
    reference: chr 16
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1872A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5153A>G
  hgvsp: ENSP00000473601.1:p.Lys1718Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5645T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4667A>G
  hgvsp: ENSP00000439819.2:p.Lys1556Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5153A>G
  hgvsp: ENSP00000449376.1:p.Lys1718Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5162A>G
  hgvsp: ENSP00000450309.1:p.Lys1721Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4226A>G
  hgvsp: ENSP00000341939.3:p.Lys1409Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1785A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*416A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5162A>G
  hgvsp: ENSP00000379654.3:p.Lys1721Arg
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys1721Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-15690622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690622
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690622
    reference: chr 16
allele count: 6
allele frequency: 4.971496751955456e-5
allele num: 120688
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5157G>A
  hgvsp: ENST00000396368.3:c.5157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5650C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5157G>A
  hgvsp: ENST00000551742.1:c.5157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*411G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5148G>A
  hgvsp: ENST00000548025.1:c.5148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4221G>A
  hgvsp: ENST00000344181.3:c.4221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4662G>A
  hgvsp: ENST00000540441.2:c.4662G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1780G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1867G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5148G>A
  hgvsp: ENST00000602337.1:c.5148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro1719Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

16-15690625-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690625
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690625
    reference: chr 16
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1864C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5145C>T
  hgvsp: ENST00000602337.1:c.5145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*408C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5145C>T
  hgvsp: ENST00000548025.1:c.5145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1777C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4659C>T
  hgvsp: ENST00000540441.2:c.4659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4218C>T
  hgvsp: ENST00000344181.3:c.4218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5154C>T
  hgvsp: ENST00000551742.1:c.5154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5154C>T
  hgvsp: ENST00000396368.3:c.5154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5653G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.488C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1718Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

16-15690633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690633
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690633
    reference: chr 16
allele count: 4
allele frequency: 3.313617310336829e-5
allele num: 120714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5661C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*400G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4210G>A
  hgvsp: ENSP00000341939.3:p.Val1404Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5137G>A
  hgvsp: ENSP00000473601.1:p.Val1713Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5137G>A
  hgvsp: ENSP00000449376.1:p.Val1713Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1769G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.480G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5146G>A
  hgvsp: ENSP00000450309.1:p.Val1716Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1856G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5146G>A
  hgvsp: ENSP00000379654.3:p.Val1716Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4651G>A
  hgvsp: ENSP00000439819.2:p.Val1551Met
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1716Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-15690634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690634
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690634
    reference: chr 16
allele count: 3
allele frequency: 2.485212982752622e-5
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5145C>T
  hgvsp: ENST00000551742.1:c.5145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4650C>T
  hgvsp: ENST00000540441.2:c.4650C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5662G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5145C>T
  hgvsp: ENST00000396368.3:c.5145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1855C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5136C>T
  hgvsp: ENST00000548025.1:c.5136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1768C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5136C>T
  hgvsp: ENST00000602337.1:c.5136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4209C>T
  hgvsp: ENST00000344181.3:c.4209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.479C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*399C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1715Pro
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

16-15690641-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690641
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690641
    reference: chr 16
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5138A>G
  hgvsp: ENSP00000379654.3:p.Lys1713Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1848A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5129A>G
  hgvsp: ENSP00000449376.1:p.Lys1710Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.472A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5129A>G
  hgvsp: ENSP00000473601.1:p.Lys1710Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4643A>G
  hgvsp: ENSP00000439819.2:p.Lys1548Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5669T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1761A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5138A>G
  hgvsp: ENSP00000450309.1:p.Lys1713Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*392A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4202A>G
  hgvsp: ENSP00000341939.3:p.Lys1401Arg
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1713Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

16-15690645-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690645
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690645
    reference: chr 16
allele count: 8
allele frequency: 6.62635633231177e-5
allele num: 120730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*388A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1844A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1757A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4639A>G
  hgvsp: ENSP00000439819.2:p.Ser1547Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5673T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5125A>G
  hgvsp: ENSP00000449376.1:p.Ser1709Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.468A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5125A>G
  hgvsp: ENSP00000473601.1:p.Ser1709Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5134A>G
  hgvsp: ENSP00000450309.1:p.Ser1712Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4198A>G
  hgvsp: ENSP00000341939.3:p.Ser1400Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5134A>G
  hgvsp: ENSP00000379654.3:p.Ser1712Gly
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1712Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-15690650-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690650
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690650
    reference: chr 16
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1752T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5120T>G
  hgvsp: ENSP00000473601.1:p.Leu1707Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4193T>G
  hgvsp: ENSP00000341939.3:p.Leu1398Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1839T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5129T>G
  hgvsp: ENSP00000450309.1:p.Leu1710Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4634T>G
  hgvsp: ENSP00000439819.2:p.Leu1545Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5120T>G
  hgvsp: ENSP00000449376.1:p.Leu1707Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5129T>G
  hgvsp: ENSP00000379654.3:p.Leu1710Arg
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5678A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*383T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.463T>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1710Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

16-15690650-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690650
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690650
    reference: chr 16
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5129T>C
  hgvsp: ENSP00000450309.1:p.Leu1710Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5120T>C
  hgvsp: ENSP00000449376.1:p.Leu1707Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5678A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.463T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4634T>C
  hgvsp: ENSP00000439819.2:p.Leu1545Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*383T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5120T>C
  hgvsp: ENSP00000473601.1:p.Leu1707Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1752T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4193T>C
  hgvsp: ENSP00000341939.3:p.Leu1398Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1839T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5129T>C
  hgvsp: ENSP00000379654.3:p.Leu1710Pro
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1710Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

16-15690652-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690652
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690652
    reference: chr 16
allele count: 2
allele frequency: 1.656561640658649e-5
allele num: 120732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*381A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5118A>T
  hgvsp: ENST00000602337.1:c.5118A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.461A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5680T>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5127A>T
  hgvsp: ENST00000551742.1:c.5127A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4632A>T
  hgvsp: ENST00000540441.2:c.4632A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1750A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4191A>T
  hgvsp: ENST00000344181.3:c.4191A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1837A>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5127A>T
  hgvsp: ENST00000396368.3:c.5127A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5118A>T
  hgvsp: ENST00000548025.1:c.5118A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1709Ser
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: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-15690654-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690654
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690654
    reference: chr 16
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5125T>C
  hgvsp: ENSP00000450309.1:p.Ser1709Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5682A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5116T>C
  hgvsp: ENSP00000449376.1:p.Ser1706Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4189T>C
  hgvsp: ENSP00000341939.3:p.Ser1397Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1835T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5125T>C
  hgvsp: ENSP00000379654.3:p.Ser1709Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5116T>C
  hgvsp: ENSP00000473601.1:p.Ser1706Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4630T>C
  hgvsp: ENSP00000439819.2:p.Ser1544Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1748T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.459T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*379T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1709Pro
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-15690657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690657
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690657
    reference: chr 16
allele count: 2
allele frequency: 1.656808655168415e-5
allele num: 120714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1832G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5122G>A
  hgvsp: ENSP00000450309.1:p.Glu1708Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5122G>A
  hgvsp: ENSP00000379654.3:p.Glu1708Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*376G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1745G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4627G>A
  hgvsp: ENSP00000439819.2:p.Glu1543Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5685C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.456G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5113G>A
  hgvsp: ENSP00000449376.1:p.Glu1705Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4186G>A
  hgvsp: ENSP00000341939.3:p.Glu1396Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5113G>A
  hgvsp: ENSP00000473601.1:p.Glu1705Lys
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1708Lys
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

16-15690657-CGGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690657
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690654
    reference: chr 16
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1829_*1831delTCC
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1742_1744delTCC
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*373_*375delTCC
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.453_455delTCC
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5110_5112delTCC
  hgvsp: ENSP00000473601.1:p.Ser1704del
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5119_5121delTCC
  hgvsp: ENSP00000379654.3:p.Ser1707del
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4624_4626delTCC
  hgvsp: ENSP00000439819.2:p.Ser1542del
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5110_5112delTCC
  hgvsp: ENSP00000449376.1:p.Ser1704del
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5688_*12+5690delAGG
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5119_5121delTCC
  hgvsp: ENSP00000450309.1:p.Ser1707del
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4183_4185delTCC
  hgvsp: ENSP00000341939.3:p.Ser1395del
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1707del
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: CGGA
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

16-15690658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690658
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690658
    reference: chr 16
allele count: 2
allele frequency: 1.656781205474005e-5
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1744C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5686G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5112C>T
  hgvsp: ENST00000602337.1:c.5112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.455C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1831C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5121C>T
  hgvsp: ENST00000396368.3:c.5121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5121C>T
  hgvsp: ENST00000551742.1:c.5121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5112C>T
  hgvsp: ENST00000548025.1:c.5112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4626C>T
  hgvsp: ENST00000540441.2:c.4626C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4185C>T
  hgvsp: ENST00000344181.3:c.4185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*375C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10565
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1707Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

16-15690663-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690663
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690663
    reference: chr 16
allele count: 2
allele frequency: 1.656891009709381e-5
allele num: 120708
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5107A>G
  hgvsp: ENSP00000473601.1:p.Thr1703Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5107A>G
  hgvsp: ENSP00000449376.1:p.Thr1703Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5116A>G
  hgvsp: ENSP00000379654.3:p.Thr1706Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1826A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5691T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4180A>G
  hgvsp: ENSP00000341939.3:p.Thr1394Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*370A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5116A>G
  hgvsp: ENSP00000450309.1:p.Thr1706Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1739A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4621A>G
  hgvsp: ENSP00000439819.2:p.Thr1541Ala
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.450A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1706Ala
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-15690666-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690666
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690666
    reference: chr 16
allele count: 7
allele frequency: 5.799695101743223e-5
allele num: 120696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5113G>A
  hgvsp: ENSP00000450309.1:p.Glu1705Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5694C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1823G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4618G>A
  hgvsp: ENSP00000439819.2:p.Glu1540Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5104G>A
  hgvsp: ENSP00000449376.1:p.Glu1702Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5104G>A
  hgvsp: ENSP00000473601.1:p.Glu1702Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5113G>A
  hgvsp: ENSP00000379654.3:p.Glu1705Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*367G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4177G>A
  hgvsp: ENSP00000341939.3:p.Glu1393Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.447G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1736G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu1705Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

16-15690667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690667
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690667
    reference: chr 16
allele count: 2
allele frequency: 1.656973372437905e-5
allele num: 120702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4176G>A
  hgvsp: ENST00000344181.3:c.4176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4617G>A
  hgvsp: ENST00000540441.2:c.4617G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1735G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1822G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5112G>A
  hgvsp: ENST00000396368.3:c.5112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5112G>A
  hgvsp: ENST00000551742.1:c.5112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5103G>A
  hgvsp: ENST00000548025.1:c.5103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5103G>A
  hgvsp: ENST00000602337.1:c.5103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*366G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5695C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.446G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7928
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1704Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

16-15690668-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690668
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690668
    reference: chr 16
allele count: 2
allele frequency: 1.657028285472833e-5
allele num: 120698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.445C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5111C>T
  hgvsp: ENSP00000379654.3:p.Ser1704Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5696G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*365C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5102C>T
  hgvsp: ENSP00000449376.1:p.Ser1701Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5111C>T
  hgvsp: ENSP00000450309.1:p.Ser1704Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5102C>T
  hgvsp: ENSP00000473601.1:p.Ser1701Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4175C>T
  hgvsp: ENSP00000341939.3:p.Ser1392Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4616C>T
  hgvsp: ENSP00000439819.2:p.Ser1539Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1734C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1821C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1704Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-15690672-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690672
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690672
    reference: chr 16
allele count: 3
allele frequency: 2.485954357877989e-5
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5700A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1817T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5107T>C
  hgvsp: ENSP00000379654.3:p.Ser1703Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5098T>C
  hgvsp: ENSP00000473601.1:p.Ser1700Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5107T>C
  hgvsp: ENSP00000450309.1:p.Ser1703Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4171T>C
  hgvsp: ENSP00000341939.3:p.Ser1391Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.441T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4612T>C
  hgvsp: ENSP00000439819.2:p.Ser1538Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*361T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5098T>C
  hgvsp: ENSP00000449376.1:p.Ser1700Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1730T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser1703Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-15690674-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690674
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690674
    reference: chr 16
allele count: 5
allele frequency: 4.142913959962879e-5
allele num: 120688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*359C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5702G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4610C>T
  hgvsp: ENSP00000439819.2:p.Pro1537Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.439C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4169C>T
  hgvsp: ENSP00000341939.3:p.Pro1390Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5105C>T
  hgvsp: ENSP00000450309.1:p.Pro1702Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5105C>T
  hgvsp: ENSP00000379654.3:p.Pro1702Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5096C>T
  hgvsp: ENSP00000473601.1:p.Pro1699Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1728C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1815C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5096C>T
  hgvsp: ENSP00000449376.1:p.Pro1699Leu
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1702Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-15690680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690680
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690680
    reference: chr 16
allele count: 2
allele frequency: 1.657220509761029e-5
allele num: 120684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5090C>T
  hgvsp: ENSP00000449376.1:p.Pro1697Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.433C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*353C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5099C>T
  hgvsp: ENSP00000450309.1:p.Pro1700Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1722C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5708G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1809C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5090C>T
  hgvsp: ENSP00000473601.1:p.Pro1697Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4604C>T
  hgvsp: ENSP00000439819.2:p.Pro1535Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4163C>T
  hgvsp: ENSP00000341939.3:p.Pro1388Leu
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5099C>T
  hgvsp: ENSP00000379654.3:p.Pro1700Leu
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10403
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro1700Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

16-15690687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690687
    reference: chr 16
allele count: 24
allele frequency: 1.989159082997663e-4
allele num: 120654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1715G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*346G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5092G>A
  hgvsp: ENSP00000379654.3:p.Val1698Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5083G>A
  hgvsp: ENSP00000473601.1:p.Val1695Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5715C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1802G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5092G>A
  hgvsp: ENSP00000450309.1:p.Val1698Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5083G>A
  hgvsp: ENSP00000449376.1:p.Val1695Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.426G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4597G>A
  hgvsp: ENSP00000439819.2:p.Val1533Met
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4156G>A
  hgvsp: ENSP00000341939.3:p.Val1386Met
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val1698Met
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-15690688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690688
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690688
    reference: chr 16
allele count: 15
allele frequency: 1.243430541969926e-4
allele num: 120634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5082C>T
  hgvsp: ENST00000548025.1:c.5082C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5091C>T
  hgvsp: ENST00000396368.3:c.5091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1714C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*345C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.425C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4596C>T
  hgvsp: ENST00000540441.2:c.4596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5082C>T
  hgvsp: ENST00000602337.1:c.5082C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5091C>T
  hgvsp: ENST00000551742.1:c.5091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1801C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5716G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4155C>T
  hgvsp: ENST00000344181.3:c.4155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro1697Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

16-15690691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690691
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690691
    reference: chr 16
allele count: 8
allele frequency: 6.630420368651372e-5
allele num: 120656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5079C>T
  hgvsp: ENST00000548025.1:c.5079C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5079C>T
  hgvsp: ENST00000602337.1:c.5079C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4152C>T
  hgvsp: ENST00000344181.3:c.4152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5088C>T
  hgvsp: ENST00000551742.1:c.5088C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5088C>T
  hgvsp: ENST00000396368.3:c.5088C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*342C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4593C>T
  hgvsp: ENST00000540441.2:c.4593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.422C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5719G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1798C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1711C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val1696Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

16-15690702-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690702
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690702
    reference: chr 16
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1787T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5068T>A
  hgvsp: ENSP00000473601.1:p.Ser1690Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*331T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5068T>A
  hgvsp: ENSP00000449376.1:p.Ser1690Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5077T>A
  hgvsp: ENSP00000379654.3:p.Ser1693Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5730A>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4582T>A
  hgvsp: ENSP00000439819.2:p.Ser1528Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4141T>A
  hgvsp: ENSP00000341939.3:p.Ser1381Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.411T>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5077T>A
  hgvsp: ENSP00000450309.1:p.Ser1693Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1700T>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1693Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-15690708-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690708
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690708
    reference: chr 16
allele count: 2
allele frequency: 1.658677370664632e-5
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4576T>G
  hgvsp: ENSP00000439819.2:p.Cys1526Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5062T>G
  hgvsp: ENSP00000449376.1:p.Cys1688Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5071T>G
  hgvsp: ENSP00000450309.1:p.Cys1691Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.405T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*325T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4135T>G
  hgvsp: ENSP00000341939.3:p.Cys1379Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1694T>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5062T>G
  hgvsp: ENSP00000473601.1:p.Cys1688Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5736A>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5071T>G
  hgvsp: ENSP00000379654.3:p.Cys1691Gly
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1781T>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys1691Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-15690711-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690711
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690711
    reference: chr 16
allele count: 6
allele frequency: 4.976857612103718e-5
allele num: 120558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1691T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5059T>C
  hgvsp: ENSP00000473601.1:p.Ser1687Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5059T>C
  hgvsp: ENSP00000449376.1:p.Ser1687Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1778T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5068T>C
  hgvsp: ENSP00000379654.3:p.Ser1690Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*322T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5739A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5068T>C
  hgvsp: ENSP00000450309.1:p.Ser1690Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4132T>C
  hgvsp: ENSP00000341939.3:p.Ser1378Pro
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.402T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4573T>C
  hgvsp: ENSP00000439819.2:p.Ser1525Pro
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10001
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1690Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

16-15690712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690712
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690712
    reference: chr 16
allele count: 1
allele frequency: 8.295175525914129e-6
allele num: 120552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1777G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5067G>A
  hgvsp: ENST00000551742.1:c.5067G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5067G>A
  hgvsp: ENST00000396368.3:c.5067G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5058G>A
  hgvsp: ENST00000548025.1:c.5058G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4131G>A
  hgvsp: ENST00000344181.3:c.4131G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5740C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*321G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.401G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5058G>A
  hgvsp: ENST00000602337.1:c.5058G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4572G>A
  hgvsp: ENST00000540441.2:c.4572G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1690G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1689Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

16-15690713-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690713
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690713
    reference: chr 16
allele count: 1
allele frequency: 8.297240337863626e-6
allele num: 120522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4130C>G
  hgvsp: ENSP00000341939.3:p.Ser1377Trp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4571C>G
  hgvsp: ENSP00000439819.2:p.Ser1524Trp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5066C>G
  hgvsp: ENSP00000450309.1:p.Ser1689Trp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.400C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1689C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5741G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*320C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5066C>G
  hgvsp: ENSP00000379654.3:p.Ser1689Trp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1776C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5057C>G
  hgvsp: ENSP00000473601.1:p.Ser1686Trp
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5057C>G
  hgvsp: ENSP00000449376.1:p.Ser1686Trp
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1689Trp
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

16-15690716-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690716
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690716
    reference: chr 16
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*317G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1686G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.397G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1773G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4568G>A
  hgvsp: ENSP00000439819.2:p.Ser1523Asn
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5063G>A
  hgvsp: ENSP00000379654.3:p.Ser1688Asn
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5744C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5054G>A
  hgvsp: ENSP00000449376.1:p.Ser1685Asn
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4127G>A
  hgvsp: ENSP00000341939.3:p.Ser1376Asn
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5063G>A
  hgvsp: ENSP00000450309.1:p.Ser1688Asn
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5054G>A
  hgvsp: ENSP00000473601.1:p.Ser1685Asn
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1688Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

16-15690718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690718
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690718
    reference: chr 16
allele count: 29
allele frequency: 2.406279559899766e-4
allele num: 120518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5052C>T
  hgvsp: ENST00000602337.1:c.5052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4566C>T
  hgvsp: ENST00000540441.2:c.4566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*315C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5061C>T
  hgvsp: ENST00000551742.1:c.5061C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4125C>T
  hgvsp: ENST00000344181.3:c.4125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5052C>T
  hgvsp: ENST00000548025.1:c.5052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1771C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5061C>T
  hgvsp: ENST00000396368.3:c.5061C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.395C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5746G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1684C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9839
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ser1687Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-15690724-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690724
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690724
    reference: chr 16
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5046T>C
  hgvsp: ENST00000602337.1:c.5046T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*309T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1678T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5055T>C
  hgvsp: ENST00000396368.3:c.5055T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4560T>C
  hgvsp: ENST00000540441.2:c.4560T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.389T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1765T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4119T>C
  hgvsp: ENST00000344181.3:c.4119T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5046T>C
  hgvsp: ENST00000548025.1:c.5046T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5055T>C
  hgvsp: ENST00000551742.1:c.5055T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5752A>G
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1685Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

16-15690728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690728
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690728
    reference: chr 16
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4115C>T
  hgvsp: ENSP00000341939.3:p.Thr1372Ile
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5051C>T
  hgvsp: ENSP00000450309.1:p.Thr1684Ile
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5042C>T
  hgvsp: ENSP00000449376.1:p.Thr1681Ile
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5051C>T
  hgvsp: ENSP00000379654.3:p.Thr1684Ile
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5042C>T
  hgvsp: ENSP00000473601.1:p.Thr1681Ile
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*305C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.385C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1674C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1761C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4556C>T
  hgvsp: ENSP00000439819.2:p.Thr1519Ile
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5756G>A
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1684Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15690730-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690730
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690730
    reference: chr 16
allele count: 1
allele frequency: 8.30137304710199e-6
allele num: 120462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*303G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4554G>A
  hgvsp: ENST00000540441.2:c.4554G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5040G>A
  hgvsp: ENST00000602337.1:c.5040G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5049G>A
  hgvsp: ENST00000551742.1:c.5049G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.383G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4113G>A
  hgvsp: ENST00000344181.3:c.4113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1759G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5040G>A
  hgvsp: ENST00000548025.1:c.5040G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5049G>A
  hgvsp: ENST00000396368.3:c.5049G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1672G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5758C>T
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1683Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

16-15690739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690739
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690739
    reference: chr 16
allele count: 2
allele frequency: 1.660908849322349e-5
allele num: 120416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4545C>T
  hgvsp: ENST00000540441.2:c.4545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5767G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5040C>T
  hgvsp: ENST00000551742.1:c.5040C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.374C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5040C>T
  hgvsp: ENST00000396368.3:c.5040C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4104C>T
  hgvsp: ENST00000344181.3:c.4104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5031C>T
  hgvsp: ENST00000548025.1:c.5031C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5031C>T
  hgvsp: ENST00000602337.1:c.5031C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1663C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1750C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1680Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-15690753-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690753
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690753
    reference: chr 16
allele count: 40
allele frequency: 3.3245233464652e-4
allele num: 120318
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5026A>G
  hgvsp: ENSP00000379654.3:p.Ile1676Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*280A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5017A>G
  hgvsp: ENSP00000473601.1:p.Ile1673Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.360A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5781T>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5026A>G
  hgvsp: ENSP00000450309.1:p.Ile1676Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1736A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4531A>G
  hgvsp: ENSP00000439819.2:p.Ile1511Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5017A>G
  hgvsp: ENSP00000449376.1:p.Ile1673Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4090A>G
  hgvsp: ENSP00000341939.3:p.Ile1364Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1649A>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9590
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8727
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ile1676Val
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

16-15690757-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690757
    reference: chr 16
allele count: 3
allele frequency: 2.494843989089216e-5
allele num: 120248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.356T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*276T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1732T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5022T>C
  hgvsp: ENST00000396368.3:c.5022T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5013T>C
  hgvsp: ENST00000548025.1:c.5013T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4086T>C
  hgvsp: ENST00000344181.3:c.4086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5022T>C
  hgvsp: ENST00000551742.1:c.5022T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1645T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5013T>C
  hgvsp: ENST00000602337.1:c.5013T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4527T>C
  hgvsp: ENST00000540441.2:c.4527T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5785A>G
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile1674Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-15690765-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690765
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690765
    reference: chr 16
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1637A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.348A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5014A>G
  hgvsp: ENSP00000450309.1:p.Met1672Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4078A>G
  hgvsp: ENSP00000341939.3:p.Met1360Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.5005A>G
  hgvsp: ENSP00000473601.1:p.Met1669Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4519A>G
  hgvsp: ENSP00000439819.2:p.Met1507Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1724A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5014A>G
  hgvsp: ENSP00000379654.3:p.Met1672Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.5005A>G
  hgvsp: ENSP00000449376.1:p.Met1669Val
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*268A>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5793T>C
  variant of: http://identifiers.org/hgnc/19213
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1672Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

16-15690774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690774
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690774
    reference: chr 16
allele count: 2
allele frequency: 1.669588446447951e-5
allele num: 119790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4510G>A
  hgvsp: ENSP00000439819.2:p.Glu1504Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*259G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4069G>A
  hgvsp: ENSP00000341939.3:p.Glu1357Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1628G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4996G>A
  hgvsp: ENSP00000473601.1:p.Glu1666Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.5005G>A
  hgvsp: ENSP00000379654.3:p.Glu1669Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4996G>A
  hgvsp: ENSP00000449376.1:p.Glu1666Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1715G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.5005G>A
  hgvsp: ENSP00000450309.1:p.Glu1669Lys
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5802C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.339G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1669Lys
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-15690788-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690788
    reference: chr 16
allele count: 9
allele frequency: 7.571041607079765e-5
allele num: 118874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1614T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4496T>C
  hgvsp: ENSP00000439819.2:p.Met1499Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.4991T>C
  hgvsp: ENSP00000379654.3:p.Met1664Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4982T>C
  hgvsp: ENSP00000473601.1:p.Met1661Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*245T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1701T>C
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4055T>C
  hgvsp: ENSP00000341939.3:p.Met1352Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4982T>C
  hgvsp: ENSP00000449376.1:p.Met1661Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.4991T>C
  hgvsp: ENSP00000450309.1:p.Met1664Thr
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5816A>G
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.325T>C
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7169
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1664Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/16-15690800-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690800
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690798
    reference: chr 16
allele count: 3
allele frequency: 2.546257002206756e-5
allele num: 117820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1695-8_*1695-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1608-8_1608-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.4985-8_4985-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4976-8_4976-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.4985-8_4985-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4976-8_4976-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.319-8_319-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*239-8_*239-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5832_*12+5833delCA
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4049-8_4049-7delGT
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4490-8_4490-7delGT
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4985-8_4985-7delGT
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: AAC
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-15690804-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690804
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690804
    reference: chr 16
allele count: 1
allele frequency: 8.510493438409559e-6
allele num: 117502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.4985-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4976-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4049-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.4985-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5832C>T
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1608-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*239-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.319-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4490-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4976-10G>A
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1695-10G>A
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4013
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

16-15690806-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690806
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690806
    reference: chr 16
allele count: 1
allele frequency: 8.514406375587495e-6
allele num: 117448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4976-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1608-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.319-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1695-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*239-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4976-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5834G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.4985-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4049-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.4985-12C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4490-12C>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

16-15690811-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690811
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690811
    reference: chr 16
allele count: 10
allele frequency: 8.536064874093044e-5
allele num: 117150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5839G>C
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.319-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1695-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4049-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.4985-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*239-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4976-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1608-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.4985-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4976-17C>G
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4490-17C>G
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3333
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-15690818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15690818
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15690818
    reference: chr 16
allele count: 34
allele frequency: 2.915801931289985e-4
allele num: 116606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449376
  ensembl transcript: ENST00000548025
  gene symbol: KIAA0430
  hgvsc: ENST00000548025.1:c.4976-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000473601
  ensembl transcript: ENST00000602337
  gene symbol: KIAA0430
  hgvsc: ENST00000602337.1:c.4976-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449329
  ensembl transcript: ENST00000552553
  gene symbol: KIAA0430
  hgvsc: ENST00000552553.1:c.*1695-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000551579
  gene symbol: KIAA0430
  hgvsc: ENST00000551579.1:n.319-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166780
  ensembl protein: ENSP00000456084
  ensembl transcript: ENST00000565857
  gene symbol: C16orf45
  hgvsc: ENST00000565857.1:c.*12+5846G>A
  variant of: http://identifiers.org/hgnc/19213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000449050
  ensembl transcript: ENST00000551878
  gene symbol: KIAA0430
  hgvsc: ENST00000551878.1:c.*239-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl transcript: ENST00000552771
  gene symbol: KIAA0430
  hgvsc: ENST00000552771.1:n.1608-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000379654
  ensembl transcript: ENST00000396368
  gene symbol: KIAA0430
  hgvsc: ENST00000396368.3:c.4985-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000450309
  ensembl transcript: ENST00000551742
  gene symbol: KIAA0430
  hgvsc: ENST00000551742.1:c.4985-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000341939
  ensembl transcript: ENST00000344181
  gene symbol: KIAA0430
  hgvsc: ENST00000344181.3:c.4049-24C>T
  variant of: http://identifiers.org/hgnc/29562
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166783
  ensembl protein: ENSP00000439819
  ensembl transcript: ENST00000540441
  gene symbol: KIAA0430
  hgvsc: ENST00000540441.2:c.4490-24C>T
  variant of: http://identifiers.org/hgnc/29562
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22210
  bin: 9.75e1
  variant carriers: 33
num of homozygotes: 0
reference allele: G

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

QD
type: SiteQuality
SIO_000300: 3.36e0

VQSLOD
type: SiteQuality
SIO_000300: -2.669e0

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.67201e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2700
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.6713e5

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.505e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.257e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.081e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.74e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.562e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.167e0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.37e-2

QD
type: SiteQuality
SIO_000300: 1.191e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

VQSLOD
type: SiteQuality
SIO_000300: -2.013e0

FS
type: SiteQuality
SIO_000300: 2.481e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.758e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.65966e5

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.724e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.152e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

DP
type: SiteQuality
SIO_000300: 1.64679e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.64e-2

GenotypeQuality
all individuals: 4024
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9421
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3588
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22360
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2604
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64330
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.37e-1

DP
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ReadPosRankSum
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SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 4.699e0

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.62e0

QD
type: SiteQuality
SIO_000300: 1.599e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64336
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.022285831118381e-4
allele num: 9782
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

FS
type: SiteQuality
SIO_000300: 9.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 2.258197e6

VQSLOD
type: SiteQuality
SIO_000300: -1.814e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 2.827e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64338
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.037129226301597e-4
allele num: 9642
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.258833e6

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 2.549e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

MQ
type: SiteQuality
SIO_000300: 5.682e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.114e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: -1.421e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8544
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: 9642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554243083618278e-5
allele num: 64340
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.581e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

FS
type: SiteQuality
SIO_000300: 2.68e0

QD
type: SiteQuality
SIO_000300: 1.17e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.258909e6

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: 9.75e1
variant carriers: 1

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: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9874
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.553422189082549e-5
allele num: 64374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
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MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: -2.266e0

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 2.260986e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.505e0

FS
type: SiteQuality
SIO_000300: 9.153e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e0

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: 7

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
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: 7
allele frequency: 1.086855261932118e-4
allele num: 64406
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 5.82e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.351e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 4.085e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.550628004341758e-5
allele num: 64490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
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allele count: 4
allele frequency: 4.139072847682119e-4
allele num: 9664
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.023e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
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 frequency: 0.0e0
allele num: 64636
num of homozygotes: 0

South Asian
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allele num: 10622
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.034340091021928e-4
allele num: 9668
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.034340091021928e-4
allele num: 9668
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64636
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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SIO_000300: 3.03e-1

MQRankSum
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SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 2.271334e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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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: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3588
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5311
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545212930341801e-5
allele num: 64716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.025e1

MQ
type: SiteQuality
SIO_000300: 5.826e1

FS
type: SiteQuality
SIO_000300: 4.983e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.254e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.855e0

DP
type: SiteQuality
SIO_000300: 2.275062e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.214e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64852
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: 3
allele frequency: 3.099173553719008e-4
allele num: 9680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

FS
type: SiteQuality
SIO_000300: 1.129e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 2.278895e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.271e1

GenotypeQuality
all individuals: 49
bin: 5.25e1
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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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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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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
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: 8586
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.033057851239669e-4
allele num: 9680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

FS
type: SiteQuality
SIO_000300: 1.129e0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.271e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
type: SiteQuality
SIO_000300: 2.278895e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.081189339084887e-5
allele num: 64910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
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: 1.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.154e1

FS
type: SiteQuality
SIO_000300: 1.803e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.281659e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: 5.83e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65798
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.023122570083896e-4
allele num: 9774
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
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: -9.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 1.542e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

QD
type: SiteQuality
SIO_000300: 1.396e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.74e0

DP
type: SiteQuality
SIO_000300: 2.316414e6

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

GenotypeQuality
all individuals: 13
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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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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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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515105602860519e-5
allele num: 66002
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14842
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.626e0

QD
type: SiteQuality
SIO_000300: 1.151e1

VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.43e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

MQRankSum
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DP
type: SiteQuality
SIO_000300: 2.32433e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.057881215052138e-4
allele num: 66170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
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: 11556
num of homozygotes: 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: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15250
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.49e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
SIO_000300: 1.114e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

DP
type: SiteQuality
SIO_000300: 2.330088e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 6.529119874640899e-5
allele num: 15316
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-2

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

QD
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SIO_000300: 1.112e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15778
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.972e-1

MQ
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MQRankSum
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InbreedingCoeff
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SIO_000300: 1.81e-2

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 2.33797e6

ReadPosRankSum
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SIO_000300: 7.9e-2

ClippingRankSum
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SIO_000300: 2.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

QD
type: SiteQuality
SIO_000300: 1.602e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16200
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: 66554
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

BaseQRankSum
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SIO_000300: 4.51e0

MQ
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SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

VQSLOD
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SIO_000300: -3.724e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e0

QD
type: SiteQuality
SIO_000300: 5.4e0

DP
type: SiteQuality
SIO_000300: 2.345105e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66674
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: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.83e-1

QD
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SIO_000300: 1.292e1

DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 8.2e-1

BaseQRankSum
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SIO_000300: 2.51e0

ClippingRankSum
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SIO_000300: -2.058e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 9.477e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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VQSLOD
type: SiteQuality
SIO_000300: -2.721e-1

DP
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.998620317327015e-5
allele num: 66682
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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

ClippingRankSum
type: SiteQuality
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VQSLOD
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.97e1

FS
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QD
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ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

FS
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

Latino
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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

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

Other
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African
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East Asian
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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
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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

Latino
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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: 3
allele frequency: 4.49829064955317e-5
allele num: 66692
num of homozygotes: 0

Other
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allele num: 900
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European (Finnish)
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num of homozygotes: 0

South Asian
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DP
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InbreedingCoeff
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FS
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 2.38e0

MQ
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SIO_000300: 5.946e1

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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Other
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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Other
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FS
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DP
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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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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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African
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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DP
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BaseQRankSum
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SIO_000300: -7.84e-1

GenotypeDepth
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variant carriers: 1

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

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

European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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South Asian
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Other
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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MQ
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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DP
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FS
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QD
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SIO_000300: 1.552e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

GenotypeDepth
all individuals: 619
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 5.25e1
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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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 5588
bin: 6.75e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.21e-1

FS
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SIO_000300: 1.122e0

InbreedingCoeff
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SIO_000300: 3.6e-3

BaseQRankSum
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MQ
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MQRankSum
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SIO_000300: 1.12e0

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 2.346879e6

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 1.552e1

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

European (Finnish)
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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: 11574
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998590662388677e-5
allele num: 66698
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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VQSLOD
type: SiteQuality
SIO_000300: -3.933e-1

InbreedingCoeff
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MQRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: 1.02e-1

FS
type: SiteQuality
SIO_000300: 2.81e0

BaseQRankSum
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SIO_000300: -5.1e-1

ClippingRankSum
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SIO_000300: -3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.876e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998590662388677e-5
allele num: 66698
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.296e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-1

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 6.79e-1

MQRankSum
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DP
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SIO_000300: 2.345379e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

GenotypeDepth
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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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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
variant carriers: 7

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

African
type: Population
allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.497151082588616e-5
allele num: 66692
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.34467e6

BaseQRankSum
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SIO_000300: -2.317e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.265e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: 1.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

GenotypeDepth
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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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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

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
all individuals: 104
bin: 2.25e1
variant carriers: 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 frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16508
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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allele frequency: 0.0e0
allele num: 900
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DP
type: SiteQuality
SIO_000300: 2.344006e6

InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 6.38e-1

MQ
type: SiteQuality
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66688
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

African
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num of homozygotes: 0

Latino
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allele frequency: 8.641548565502938e-5
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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East Asian
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423361201987156e-4
allele num: 16506
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

FS
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.286e1

DP
type: SiteQuality
SIO_000300: 2.341313e6

GenotypeDepth
all individuals: 617
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 7.75e1
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GenotypeQuality
all individuals: 3574
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
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: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.885e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 2.338134e6

QD
type: SiteQuality
SIO_000300: 1.093e1

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

GenotypeDepth
all individuals: 547
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3993
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 23

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 3570
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 20
allele frequency: 1.728907330567082e-3
allele num: 11568
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999940001199976e-5
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.232142857142857e-3
allele num: 896
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 2.335516e6

QD
type: SiteQuality
SIO_000300: 1.501e1

GenotypeDepth
all individuals: 619
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 14290
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 156
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 5437
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 4115
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variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22217
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 9790
num of homozygotes: 0

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

South Asian
type: Population
allele count: 15
allele frequency: 9.088705768298595e-4
allele num: 16504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.48e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

BaseQRankSum
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SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

DP
type: SiteQuality
SIO_000300: 2.334541e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 171
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GenotypeQuality
all individuals: 218
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GenotypeQuality
all individuals: 3981
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 3119
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 142
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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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GenotypeQuality
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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: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2559
bin: 8.75e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 14247
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.999550022498874e-5
allele num: 66670
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.764e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -4.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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SIO_000300: 1.17e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.27e-1

GenotypeDepth
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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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GenotypeQuality
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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
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GenotypeQuality
all individuals: 22179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4102
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
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: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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VQSLOD
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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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MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 22167
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 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: 9788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002371873780286e-5
allele num: 66614
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

DP
type: SiteQuality
SIO_000300: 2.322756e6

GenotypeDepth
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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
all individuals: 237
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 13905
bin: 6.25e1
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GenotypeQuality
all individuals: 9
bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.595604775912787e-4
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
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SIO_000300: -7.02e-1

DP
type: SiteQuality
SIO_000300: 2.320057e6

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 1.809e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

QD
type: SiteQuality
SIO_000300: 1.489e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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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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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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQRankSum
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SIO_000300: -2.94e-1

QD
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BaseQRankSum
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SIO_000300: 7.04e-1

ReadPosRankSum
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SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 1.061e0

DP
type: SiteQuality
SIO_000300: 2.319491e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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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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GenotypeQuality
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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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bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.18e1

InbreedingCoeff
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SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.4337e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-2

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 2.318887e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 7.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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: 1
allele frequency: 1.02291325695581e-4
allele num: 9776
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

East 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: 9.06e-1

FS
type: SiteQuality
SIO_000300: 4.595e0

MQRankSum
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SIO_000300: 3.0e-2

QD
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SIO_000300: 1.437e1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
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SIO_000300: 1.53e0

BaseQRankSum
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SIO_000300: -4.367e0

DP
type: SiteQuality
SIO_000300: 2.317217e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.389e0

GenotypeDepth
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variant carriers: 1

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: 29

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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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: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3909
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.355531525036797e-4
allele num: 66582
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.374e0

MQ
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SIO_000300: 5.956e1

DP
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MQRankSum
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QD
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
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SIO_000300: 3.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
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SIO_000300: 4.6e-1

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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: 3559
bin: 9.25e1
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: 8590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
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

South Asian
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allele num: 16502
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VQSLOD
type: SiteQuality
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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MQRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

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

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

European (Finnish)
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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: 8584
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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.02e-1

BaseQRankSum
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SIO_000300: -2.655e0

QD
type: SiteQuality
SIO_000300: 1.318e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

DP
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SIO_000300: 2.311417e6

FS
type: SiteQuality
SIO_000300: 7.653e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 303
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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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bin: 6.25e1
variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 306
bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

FS
type: SiteQuality
SIO_000300: 1.905e0

VQSLOD
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ReadPosRankSum
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SIO_000300: 7.61e-1

QD
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InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
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SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 2.309667e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 39

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

African
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allele count: 7
allele frequency: 7.185382878259084e-4
allele num: 9742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
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allele count: 32
allele frequency: 1.941747572815534e-3
allele num: 16480
num of homozygotes: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.98e0

DP
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SIO_000300: 2.308407e6

MQRankSum
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SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
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SIO_000300: 3.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

QD
type: SiteQuality
SIO_000300: 1.465e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 83
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3955
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GenotypeQuality
all individuals: 4081
bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
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: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.517391959042313e-5
allele num: 66410
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.306603e6

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 13753
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22164
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variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.032417922775139e-4
allele num: 9686
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66332
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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

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

East Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
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DP
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MQ
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.97e0

ReadPosRankSum
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SIO_000300: 2.14e0

BaseQRankSum
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SIO_000300: 5.14e0

QD
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SIO_000300: 3.065e1

GenotypeDepth
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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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GenotypeQuality
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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: 185
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.019961948479449e-5
allele num: 66226
num of homozygotes: 1

Other
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BaseQRankSum
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SIO_000300: -1.733e0

ReadPosRankSum
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.728e1

MQRankSum
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ClippingRankSum
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SIO_000300: -1.733e0

QD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8
allele frequency: 9.313154831199069e-4
allele num: 8590
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.042318115488847e-4
allele num: 9594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15754
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Latino
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Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 193
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GenotypeQuality
all individuals: 3595
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.575542201750907e-5
allele num: 65566
num of homozygotes: 0

Latino
type: Population
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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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South Asian
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African
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allele count: 0
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ClippingRankSum
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SIO_000300: -6.53e-1

MQRankSum
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QD
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SIO_000300: 1.318e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.886e0

MQ
type: SiteQuality
SIO_000300: 6.034e1

DP
type: SiteQuality
SIO_000300: 2.262251e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 2972
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4691
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22184
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14946
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: 9506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527510463446675e-5
allele num: 65466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e0

DP
type: SiteQuality
SIO_000300: 2.257215e6

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 4.547e0

QD
type: SiteQuality
SIO_000300: 9.75e0

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
all individuals: 350
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3093
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3597
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4012
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3044
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22185
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527837193668643e-5
allele num: 65452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14922
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: 11532
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 3.668e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 2.254276e6

QD
type: SiteQuality
SIO_000300: 1.179e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4649
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22190
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.377073260297448e-4
allele num: 65356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

QD
type: SiteQuality
SIO_000300: 1.043e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 4.315e0

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

DP
type: SiteQuality
SIO_000300: 2.245866e6

GenotypeQuality
all individuals: 3032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9411
bin: 6.25e1
variant carriers: 0