X-129364665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364665
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364665
    reference: chr 0
allele count: 1
allele frequency: 1.148488015527558e-5
allele num: 87071
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.808G>A
  hgvsp: ENSP00000408521.1:p.Val270Ile
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.808G>A
  hgvsp: ENSP00000360017.4:p.Val270Ile
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val270Ile
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9283
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-129364676-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364676
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364676
    reference: chr 0
allele count: 1
allele frequency: 1.157956900844151e-5
allele num: 86359
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.797A>C
  hgvsp: ENSP00000408521.1:p.Lys266Thr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.797A>C
  hgvsp: ENSP00000360017.4:p.Lys266Thr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Lys266Thr
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.191327138432213e-4
  allele num: 8394
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

X-129364683-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364683
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364683
    reference: chr 0
allele count: 1
allele frequency: 1.166207958203107e-5
allele num: 85748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.790A>G
  hgvsp: ENSP00000408521.1:p.Ile264Val
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.790A>G
  hgvsp: ENSP00000360017.4:p.Ile264Val
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile264Val
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9237
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

X-129364708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364708
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364708
    reference: chr 0
allele count: 1
allele frequency: 1.235574665777053e-5
allele num: 80934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-7C>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-7C>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: c.772-7C>T
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6343
  num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

X-129364711-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364711
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364712
    reference: chr 0
allele count: 1
allele frequency: 1.253054319904768e-5
allele num: 79805
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-11dupT
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-11dupT
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.131605748557203e-4
  allele num: 8837
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

X-129364715-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364715
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364715
    reference: chr 0
allele count: 1
allele frequency: 1.26270597891281e-5
allele num: 79195
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-14T>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-14T>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8785
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
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site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-129364718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364718
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364718
    reference: chr 0
allele count: 1
allele frequency: 1.276487107480214e-5
allele num: 78340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-17T>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-17T>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
  type: Population
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  allele num: 7887
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

X-129364722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364722
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364722
    reference: chr 0
allele count: 1
allele frequency: 1.299376299376299e-5
allele num: 76960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-21C>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-21C>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Other
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  allele num: 555
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population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
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X-129364722-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364722
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364722
    reference: chr 0
allele count: 1
allele frequency: 1.299376299376299e-5
allele num: 76960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-21C>A
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-21C>A
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 24912
  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8624
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

X-129364724-GCCTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364724
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364720
    reference: chr 0
allele count: 1
allele frequency: 1.310015065173249e-5
allele num: 76335
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-27_772-24delAAGG
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-27_772-24delAAGG
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4270
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: GCCTT
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

X-129364731-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364731
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364731
    reference: chr 0
allele count: 1
allele frequency: 1.352832154114639e-5
allele num: 73919
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-30G>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-30G>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 182
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.456942089874941e-5
  allele num: 40701
  num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
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X-129364732-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364732
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364732
    reference: chr 0
allele count: 1
allele frequency: 1.364424008404852e-5
allele num: 73291
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-31A>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-31A>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8364
  num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

X-129364732-T-TGTAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364732
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364736
    reference: chr 0
allele count: 1
allele frequency: 1.364424008404852e-5
allele num: 73291
alternate allele: TGTAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-32_772-31insTTAC
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-32_772-31insTTAC
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8364
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

X-129364734-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364734
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364734
    reference: chr 0
allele count: 1
allele frequency: 1.372438686301689e-5
allele num: 72863
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-33G>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-33G>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 535
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

X-129364751-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364751
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364751
    reference: chr 0
allele count: 5
allele frequency: 7.61556621734826e-5
allele num: 65655
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-50T>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-50T>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3952
  num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

X-129364753-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129364753
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129364753
    reference: chr 0
allele count: 1
allele frequency: 1.544640098856966e-5
allele num: 64740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.772-52T>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.772-52T>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 1.905487804878049e-4
  allele num: 5248
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

X-129370141-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370141
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370141
    reference: chr 0
allele count: 1
allele frequency: 1.427572128081771e-5
allele num: 70049
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+47C>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+47C>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6385
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

X-129370142-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370142
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370142
    reference: chr 0
allele count: 1
allele frequency: 1.422151430684339e-5
allele num: 70316
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+46C>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+46C>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6413
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
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X-129370144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370144
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370144
    reference: chr 0
allele count: 3
allele frequency: 4.246464818038983e-5
allele num: 70647
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+44A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+44A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
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  allele num: 5611
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population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

X-129370148-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370148
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370148
    reference: chr 0
allele count: 1
allele frequency: 1.41001959927243e-5
allele num: 70921
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+40A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+40A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
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  allele num: 8405
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population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

X-129370148-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370148
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370147
    reference: chr 0
allele count: 1
allele frequency: 1.41001959927243e-5
allele num: 70921
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+39delT
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+39delT
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 38476
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: TA
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

X-129370151-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370151
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370151
    reference: chr 0
allele count: 1
allele frequency: 1.403745192172717e-5
allele num: 71238
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+37T>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+37T>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 525
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

X-129370155-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370155
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370155
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 71671
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+33A>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+33A>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
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  allele num: 5708
  num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
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site quality: DP
site quality: FS
site quality: MQ
site quality: QD
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site quality: VQSLOD

X-129370165-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370165
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370165
    reference: chr 0
allele count: 1
allele frequency: 1.339710354621331e-5
allele num: 74643
alternate allele: A
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+23A>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+23A>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: South Asian
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  allele num: 6998
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population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

X-129370165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370165
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370165
    reference: chr 0
allele count: 31
allele frequency: 4.153102099326126e-4
allele num: 74643
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+23A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+23A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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population: Other
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  allele num: 547
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population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
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site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
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site quality: QD

X-129370166-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370166
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370166
    reference: chr 0
allele count: 1
allele frequency: 1.331327466616964e-5
allele num: 75113
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.771+22A>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.771+22A>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6007
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

X-129370194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370194
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370194
    reference: chr 0
allele count: 1
allele frequency: 1.171797185343161e-5
allele num: 85339
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.765C>T
  hgvsp: ENST00000447817.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.765C>T
  hgvsp: ENST00000370978.4:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.His255His
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.084245906971701e-4
  allele num: 9223
  num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-129370211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370211
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370211
    reference: chr 0
allele count: 1
allele frequency: 1.151927751091452e-5
allele num: 86811
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.748G>A
  hgvsp: ENSP00000360017.4:p.Asp250Asn
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.748G>A
  hgvsp: ENSP00000408521.1:p.Asp250Asn
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40924
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asp250Asn
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8365
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD

X-129370231-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370231
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370231
    reference: chr 0
allele count: 1
allele frequency: 1.14646030381198e-5
allele num: 87225
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.728A>G
  hgvsp: ENSP00000360017.4:p.Asn243Ser
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.728A>G
  hgvsp: ENSP00000408521.1:p.Asn243Ser
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asn243Ser
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8427
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

X-129370247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370247
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370247
    reference: chr 0
allele count: 1
allele frequency: 1.146486591839308e-5
allele num: 87223
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.712G>A
  hgvsp: ENSP00000360017.4:p.Ala238Thr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.712G>A
  hgvsp: ENSP00000408521.1:p.Ala238Thr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ala238Thr
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9295
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

X-129370270-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370270
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370270
    reference: chr 0
allele count: 6
allele frequency: 6.914912007744702e-5
allele num: 86769
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.689A>G
  hgvsp: ENSP00000360017.4:p.Asp230Gly
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.689A>G
  hgvsp: ENSP00000408521.1:p.Asp230Gly
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 696
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  variant carriers: 0
hgvs: p.Asp230Gly
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 627
  num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-129370272-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370272
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370272
    reference: chr 0
allele count: 39
allele frequency: 4.499255892294736e-4
allele num: 86681
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.687T>C
  hgvsp: ENST00000370978.4:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.687T>C
  hgvsp: ENST00000447817.1:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 396
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  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 73
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  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1766
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  variant carriers: 0
hgvs: p.Tyr229Tyr
num of homozygotes: 0
population: African
  type: Population
  allele count: 34
  allele frequency: 4.054859868813357e-3
  allele num: 8385
  num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

X-129370275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370275
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370275
    reference: chr 0
allele count: 1
allele frequency: 1.155241329913819e-5
allele num: 86562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.684A>G
  hgvsp: ENST00000447817.1:c.684A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.684A>G
  hgvsp: ENST00000370978.4:c.684A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1201
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hgvs: p.Pro228Pro
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9848
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

X-129370282-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370282
    reference: chr 0
allele count: 1
allele frequency: 1.16185850887079e-5
allele num: 86069
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.677C>T
  hgvsp: ENSP00000360017.4:p.Ser226Leu
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.677C>T
  hgvsp: ENSP00000408521.1:p.Ser226Leu
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ser226Leu
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6585
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

X-129370284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370284
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370284
    reference: chr 0
allele count: 1
allele frequency: 1.164171459172507e-5
allele num: 85898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.675C>T
  hgvsp: ENST00000447817.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.675C>T
  hgvsp: ENST00000370978.4:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 39694
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr225Thr
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6574
  num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

X-129370284-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370284
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370284
    reference: chr 0
allele count: 6
allele frequency: 6.985028755035041e-5
allele num: 85898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.675C>A
  hgvsp: ENST00000447817.1:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.675C>A
  hgvsp: ENST00000370978.4:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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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  variant carriers: 0
hgvs: p.Thr225Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4503
  num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

X-129370305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370305
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370305
    reference: chr 0
allele count: 1
allele frequency: 1.206345376681344e-5
allele num: 82895
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.665-11A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.665-11A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9115
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-129370308-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370308
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370308
    reference: chr 0
allele count: 1
allele frequency: 1.205952581944478e-5
allele num: 82922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.665-14T>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.665-14T>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4454
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

X-129370312-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370312
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370312
    reference: chr 0
allele count: 1
allele frequency: 1.209935994385897e-5
allele num: 82649
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.665-18G>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.665-18G>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
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  allele num: 8013
  num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

X-129370325-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
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    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370325
    reference: chr 0
allele count: 1
allele frequency: 1.225925880521264e-5
allele num: 81571
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.665-31T>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.665-31T>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele num: 4424
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

X-129370327-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370327
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370327
    reference: chr 0
allele count: 1
allele frequency: 1.231238995801475e-5
allele num: 81219
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.665-33A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.665-33A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  allele num: 9055
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population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
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site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
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X-129370337-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370337
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370337
    reference: chr 0
allele count: 3
allele frequency: 3.750703256860662e-5
allele num: 79985
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.665-43A>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.665-43A>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
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site quality: FS
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site quality: MQ
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site quality: DP
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site quality: QD

X-129370396-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370396
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370396
    reference: chr 0
allele count: 8
allele frequency: 1.074431222971339e-4
allele num: 74458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+47A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+47A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8989
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

X-129370404-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370404
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370403
    reference: chr 0
allele count: 35
allele frequency: 4.640186668080819e-4
allele num: 75428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+38delT
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+38delT
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 1.803751803751804e-4
  allele num: 5544
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: TA
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

X-129370410-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370410
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370409
    reference: chr 0
allele count: 16
allele frequency: 2.091038592731027e-4
allele num: 76517
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+32delT
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+32delT
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 9
  allele frequency: 1.577287066246057e-3
  allele num: 5706
  num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: TA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

X-129370411-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370411
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370412
    reference: chr 0
allele count: 8
allele frequency: 1.148270417683364e-4
allele num: 69670
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+31dupA
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+31dupA
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14348
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.454333915066899e-4
  allele num: 6876
  num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

X-129370411-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370411
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370410
    reference: chr 0
allele count: 169
allele frequency: 2.425721257356107e-3
allele num: 69670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+31delA
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+31delA
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 99
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  variant carriers: 3
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 6
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 50
  allele frequency: 1.288261362465217e-3
  allele num: 38812
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: AT
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

X-129370412-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370412
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370412
    reference: chr 0
allele count: 1
allele frequency: 1.437711163827187e-5
allele num: 69555
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+31A>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+31A>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
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  allele frequency: 1.441129845799107e-4
  allele num: 6939
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
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site quality: ReadPosRankSum

X-129370412-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370412
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370412
    reference: chr 0
allele count: 1
allele frequency: 1.437711163827187e-5
allele num: 69555
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+31A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+31A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
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  allele num: 5271
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

X-129370413-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370413
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370413
    reference: chr 0
allele count: 1
allele frequency: 1.364684689602467e-5
allele num: 73277
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+30A>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+30A>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
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site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
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X-129370420-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370420
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370420
    reference: chr 0
allele count: 2
allele frequency: 2.46020616527665e-5
allele num: 81294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+23A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+23A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
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  allele num: 7938
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population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
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site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
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site quality: VQSLOD

X-129370420-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370420
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370420
    reference: chr 0
allele count: 1
allele frequency: 1.230103082638325e-5
allele num: 81294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+23A>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+23A>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 597
  num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
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site quality: DP
site quality: QD

X-129370421-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370421
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370421
    reference: chr 0
allele count: 1
allele frequency: 1.22591085176286e-5
allele num: 81572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+22T>C
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+22T>C
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.2465719272002e-4
  allele num: 8022
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-129370422-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370422
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370422
    reference: chr 0
allele count: 4
allele frequency: 4.871395167575994e-5
allele num: 82112
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+21G>T
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+21G>T
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8124
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-129370436-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370436
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370436
    reference: chr 0
allele count: 4
allele frequency: 4.716814263646333e-5
allele num: 84803
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.664+7A>G
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.664+7A>G
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.664+7A>G
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6594
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

X-129370454-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370454
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370454
    reference: chr 0
allele count: 1
allele frequency: 1.162925921618793e-5
allele num: 85990
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.653T>C
  hgvsp: ENSP00000360017.4:p.Met218Thr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.653T>C
  hgvsp: ENSP00000408521.1:p.Met218Thr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Met218Thr
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6615
  num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

X-129370462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370462
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370462
    reference: chr 0
allele count: 88
allele frequency: 1.019202705519909e-3
allele num: 86342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.645C>T
  hgvsp: ENST00000370978.4:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.645C>T
  hgvsp: ENST00000447817.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ser215Ser
num of homozygotes: 1
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6621
  num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

X-129370463-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370463
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370463
    reference: chr 0
allele count: 1
allele frequency: 1.157621781811447e-5
allele num: 86384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.644C>A
  hgvsp: ENSP00000408521.1:p.Ser215Tyr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.644C>A
  hgvsp: ENSP00000360017.4:p.Ser215Tyr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ser215Tyr
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 623
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

X-129370469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370469
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370469
    reference: chr 0
allele count: 1
allele frequency: 1.155268022181146e-5
allele num: 86560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.638C>T
  hgvsp: ENSP00000408521.1:p.Thr213Ile
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.638C>T
  hgvsp: ENSP00000360017.4:p.Thr213Ile
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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hgvs: p.Thr213Ile
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47704
  num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
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site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-129370474-TGGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370474
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370471
    reference: chr 0
allele count: 2
allele frequency: 2.305581813570655e-5
allele num: 86746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.630_632delTCC
  hgvsp: ENSP00000408521.1:p.Pro211del
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.630_632delTCC
  hgvsp: ENSP00000360017.4:p.Pro211del
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro211del
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8508
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: TGGA
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

X-129370484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370484
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370484
    reference: chr 0
allele count: 1
allele frequency: 1.148936659121983e-5
allele num: 87037
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.623G>A
  hgvsp: ENSP00000360017.4:p.Gly208Asp
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.623G>A
  hgvsp: ENSP00000408521.1:p.Gly208Asp
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 65
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  variant carriers: 0
hgvs: p.Gly208Asp
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6630
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

X-129370485-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370485
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370485
    reference: chr 0
allele count: 1
allele frequency: 1.148725489069877e-5
allele num: 87053
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.622G>T
  hgvsp: ENSP00000360017.4:p.Gly208Cys
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.622G>T
  hgvsp: ENSP00000408521.1:p.Gly208Cys
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1092
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gly208Cys
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 629
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

X-129370486-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370486
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370486
    reference: chr 0
allele count: 36
allele frequency: 4.133797237245513e-4
allele num: 87087
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.621T>G
  hgvsp: ENSP00000408521.1:p.Ile207Met
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.621T>G
  hgvsp: ENSP00000360017.4:p.Ile207Met
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile207Met
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4521
  num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-129370498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370498
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370498
    reference: chr 0
allele count: 1
allele frequency: 1.14593479631009e-5
allele num: 87265
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.609A>G
  hgvsp: ENST00000447817.1:c.609A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.609A>G
  hgvsp: ENST00000370978.4:c.609A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 262
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 47903
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser203Ser
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6632
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

X-129370505-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370505
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370505
    reference: chr 0
allele count: 1
allele frequency: 1.144872117784444e-5
allele num: 87346
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.602C>G
  hgvsp: ENSP00000360017.4:p.Ser201Cys
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.602C>G
  hgvsp: ENSP00000408521.1:p.Ser201Cys
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ser201Cys
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 632
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

X-129370515-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370515
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370515
    reference: chr 0
allele count: 1
allele frequency: 1.144688644688645e-5
allele num: 87360
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.592A>C
  hgvsp: ENSP00000360017.4:p.Ile198Leu
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.592A>C
  hgvsp: ENSP00000408521.1:p.Ile198Leu
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile198Leu
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 631
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

X-129370521-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370521
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370521
    reference: chr 0
allele count: 1
allele frequency: 1.144727955401399e-5
allele num: 87357
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.586C>A
  hgvsp: ENSP00000408521.1:p.Pro196Thr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.586C>A
  hgvsp: ENSP00000360017.4:p.Pro196Thr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Pro196Thr
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9299
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS

X-129370524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370524
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370524
    reference: chr 0
allele count: 1
allele frequency: 1.144806584927476e-5
allele num: 87351
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.583G>A
  hgvsp: ENSP00000360017.4:p.Val195Ile
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.583G>A
  hgvsp: ENSP00000408521.1:p.Val195Ile
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Val195Ile
num of homozygotes: 0
population: South Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 10000
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

X-129370535-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370535
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370535
    reference: chr 0
allele count: 1
allele frequency: 1.145764110085016e-5
allele num: 87278
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.572C>T
  hgvsp: ENSP00000360017.4:p.Thr191Ile
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.572C>T
  hgvsp: ENSP00000408521.1:p.Thr191Ile
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 686
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr191Ile
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9986
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-129370540-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370540
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370540
    reference: chr 0
allele count: 1
allele frequency: 1.146894210478026e-5
allele num: 87192
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.567A>G
  hgvsp: ENST00000370978.4:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.567A>G
  hgvsp: ENST00000447817.1:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 253
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro189Pro
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 629
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

X-129370541-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370541
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370541
    reference: chr 0
allele count: 1
allele frequency: 1.147117866360769e-5
allele num: 87175
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.566C>T
  hgvsp: ENSP00000408521.1:p.Pro189Leu
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.566C>T
  hgvsp: ENSP00000360017.4:p.Pro189Leu
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 5701
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
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genotype quality: GenotypeQuality
  all individuals: 818
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 105
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  variant carriers: 0
hgvs: p.Pro189Leu
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9951
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

X-129370542-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370542
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370541
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87111
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.564delA
  hgvsp: ENSP00000360017.4:p.Lys188AsnfsTer11
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.564delA
  hgvsp: ENSP00000408521.1:p.Lys188AsnfsTer11
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 20910
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 527
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Lys188AsnfsTer11
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9942
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: GT
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

X-129370548-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370548
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370548
    reference: chr 0
allele count: 1
allele frequency: 1.148488015527558e-5
allele num: 87071
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.559A>G
  hgvsp: ENSP00000408521.1:p.Lys187Glu
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.559A>G
  hgvsp: ENSP00000360017.4:p.Lys187Glu
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Lys187Glu
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8503
  num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS

X-129370599-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370599
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370599
    reference: chr 0
allele count: 21
allele frequency: 2.574381229083153e-4
allele num: 81573
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.508T>A
  hgvsp: ENSP00000408521.1:p.Ser170Thr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.508T>A
  hgvsp: ENSP00000360017.4:p.Ser170Thr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser170Thr
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8247
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
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site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-129370604-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370604
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370604
    reference: chr 0
allele count: 1
allele frequency: 1.245578197399233e-5
allele num: 80284
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.503A>T
  hgvsp: ENSP00000360017.4:p.Asn168Ile
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.503A>T
  hgvsp: ENSP00000408521.1:p.Asn168Ile
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asn168Ile
num of homozygotes: 0
population: African
  type: Population
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  allele frequency: 0.0e0
  allele num: 8187
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

X-129370607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370607
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370607
    reference: chr 0
allele count: 1
allele frequency: 1.258716612541852e-5
allele num: 79446
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.500A>G
  hgvsp: ENSP00000360017.4:p.Lys167Arg
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.500A>G
  hgvsp: ENSP00000408521.1:p.Lys167Arg
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Lys167Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.131733816206428e-4
  allele num: 8836
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

X-129370609-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370609
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370609
    reference: chr 0
allele count: 1
allele frequency: 1.270357478594477e-5
allele num: 78718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.498G>C
  hgvsp: ENSP00000408521.1:p.Met166Ile
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.498G>C
  hgvsp: ENSP00000360017.4:p.Met166Ile
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4648
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31450
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met166Ile
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 1.6e-4
  allele num: 6250
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-129370610-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129370610
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129370610
    reference: chr 0
allele count: 1
allele frequency: 1.278232970741247e-5
allele num: 78233
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000408521
  ensembl transcript: ENST00000447817
  gene symbol: ZNF280C
  hgvsc: ENST00000447817.1:c.497T>C
  hgvsp: ENSP00000408521.1:p.Met166Thr
  variant of: http://identifiers.org/hgnc/25955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000056277
  ensembl protein: ENSP00000360017
  ensembl transcript: ENST00000370978
  gene symbol: ZNF280C
  hgvsc: ENST00000370978.4:c.497T>C
  hgvsp: ENSP00000360017.4:p.Met166Thr
  variant of: http://identifiers.org/hgnc/25955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4609
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met166Thr
num of homozygotes: 0
reference allele: A

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47728
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.016570092507878e-4
allele num: 9837
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.963e0

QD
type: SiteQuality
SIO_000300: 1.013e1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.273e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-2

DP
type: SiteQuality
SIO_000300: 1.416724e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9535
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9263
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.428e1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

FS
type: SiteQuality
SIO_000300: 5.771e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

DP
type: SiteQuality
SIO_000300: 1.396336e6

VQSLOD
type: SiteQuality
SIO_000300: 8.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.121655740139605e-5
allele num: 47133
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 2.736e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.09e-2

DP
type: SiteQuality
SIO_000300: 1.378998e6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4381
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.233501911927963e-4
allele num: 8107
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44567
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8933
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 579
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.603e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 1.242029e6

VQSLOD
type: SiteQuality
SIO_000300: -2.646e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43955
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4355
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7845
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7963
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 4.896e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.041e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.225596e6

QD
type: SiteQuality
SIO_000300: 1.622e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.06e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4334
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.293326435592343e-4
allele num: 7732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6213
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 571
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.731e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 7.291e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.139e-1

DP
type: SiteQuality
SIO_000300: 1.184801e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7575
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4309
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 567
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.31878681074062e-5
allele num: 43126
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 1.158598e6

MQ
type: SiteQuality
SIO_000300: 3.211e1

QD
type: SiteQuality
SIO_000300: 9.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.963e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.362334931846637e-5
allele num: 42331
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6059
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7301
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.539e0

QD
type: SiteQuality
SIO_000300: 3.65e0

DP
type: SiteQuality
SIO_000300: 1.117094e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 6.368e0

MQ
type: SiteQuality
SIO_000300: 3.435e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.659e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.175e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4276
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7301
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6059
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.362334931846637e-5
allele num: 42331
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 555
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.175e0

MQ
type: SiteQuality
SIO_000300: 3.435e1

MQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.659e0

FS
type: SiteQuality
SIO_000300: 6.368e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -5.539e0

DP
type: SiteQuality
SIO_000300: 1.117094e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7155
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.381973226620933e-5
allele num: 41982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7775
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8587
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.992e0

FS
type: SiteQuality
SIO_000300: 2.281e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.214e0

VQSLOD
type: SiteQuality
SIO_000300: -1.781e0

MQ
type: SiteQuality
SIO_000300: 3.837e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 1.09813e6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5857
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4217
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South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.435e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 3.813e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

South Asian
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allele frequency: 1.539408866995074e-4
allele num: 6496
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African
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allele frequency: 0.0e0
allele num: 7556
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40308
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Other
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allele frequency: 0.0e0
allele num: 532
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5828
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4207
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.766e0

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e0

VQSLOD
type: SiteQuality
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MQ
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
SIO_000300: 3.68e0

European (Non-Finnish)
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allele frequency: 2.480897092388608e-5
allele num: 40308
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4207
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African
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allele frequency: 0.0e0
allele num: 7556
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Other
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allele num: 532
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

South Asian
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allele count: 0
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allele num: 6496
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MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.766e0

DP
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.356e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.893e0

South Asian
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allele frequency: 1.560305819940708e-4
allele num: 6409
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 8347
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 40078
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5776
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 7532
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.21e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 1.011777e6

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7635
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5246
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5296
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7146
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 479
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European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.392718865769756e-4
allele num: 35901
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.35984e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.375e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.043e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 473
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35363
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African
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allele count: 0
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Latino
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South Asian
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QD
type: SiteQuality
SIO_000300: 1.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.135e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 9.40194e5

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 514
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5580
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4107
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 7177
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.635879593020191e-5
allele num: 37938
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DP
type: SiteQuality
SIO_000300: 1.153052e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 2.991e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 519
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.623157232044489e-5
allele num: 38122
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 4123
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.644e0

DP
type: SiteQuality
SIO_000300: 1.161526e6

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38315
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 4.639653572533251e-4
allele num: 6466
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4129
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.279e1

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

South Asian
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allele count: 0
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African
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allele count: 1
allele frequency: 1.38217000691085e-4
allele num: 7235
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38476
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4132
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Other
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4132
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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African
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allele frequency: 1.38217000691085e-4
allele num: 7235
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Other
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South Asian
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allele num: 6519
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QD
type: SiteQuality
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele count: 0
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South Asian
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allele frequency: 1.525553012967201e-4
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African
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DP
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QD
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MQ
type: SiteQuality
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FS
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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Other
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African
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South Asian
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Latino
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allele frequency: 0.0e0
allele num: 8457
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European (Non-Finnish)
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allele count: 0
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European (Finnish)
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
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FS
type: SiteQuality
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MQ
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QD
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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Latino
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African
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allele frequency: 0.0e0
allele num: 7472
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 5968
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40756
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Other
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FS
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VQSLOD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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European (Non-Finnish)
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allele frequency: 6.13406614976936e-4
allele num: 40756
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African
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European (Finnish)
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allele num: 4225
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South Asian
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Latino
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allele frequency: 4.609888210210903e-4
allele num: 8677
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East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4247
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Latino
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Other
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African
type: Population
allele count: 0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.436587802441461e-5
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South Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
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FS
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
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Other
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allele count: 0
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African
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allele count: 0
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.763e0

QD
type: SiteQuality
SIO_000300: 1.297e1

DP
type: SiteQuality
SIO_000300: 1.571519e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.85e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6619
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9275
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.103226349219703e-5
allele num: 47546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9867
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.81e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.797e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.600451e6

VQSLOD
type: SiteQuality
SIO_000300: 2.19e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47730
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10001
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VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

FS
type: SiteQuality
SIO_000300: 1.942e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.63e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.693e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

DP
type: SiteQuality
SIO_000300: 1.609106e6

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.095513505584544e-5
allele num: 47721
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8425
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.369e0

MQRankSum
type: SiteQuality
SIO_000300: -9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.696e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.609091e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8387
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.264515585154587e-4
allele num: 47449
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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allele num: 9898
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MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

QD
type: SiteQuality
SIO_000300: 1.47e1

FS
type: SiteQuality
SIO_000300: 2.583e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.593152e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.59e-1

East Asian
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: 9879
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.314529177003559e-4
allele num: 9271
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.110060769750169e-5
allele num: 47392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-1

QD
type: SiteQuality
SIO_000300: 1.719e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

DP
type: SiteQuality
SIO_000300: 1.59191e6

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.112601668955319e-5
allele num: 47335
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8363
num of homozygotes: 0

East Asian
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: 624
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 1.128e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.585287e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.668e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9245
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.12544368636953e-5
allele num: 47049
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8331
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.24e0

MQRankSum
type: SiteQuality
SIO_000300: 9.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.711e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.81e-1

DP
type: SiteQuality
SIO_000300: 1.565232e6

QD
type: SiteQuality
SIO_000300: 1.107e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9239
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.130469981677958e-5
allele num: 46938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.97e-2

QD
type: SiteQuality
SIO_000300: 1.699e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

DP
type: SiteQuality
SIO_000300: 1.558971e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9239
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.211538461538462e-4
allele num: 8320
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46938
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

QD
type: SiteQuality
SIO_000300: 1.699e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.558971e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.97e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4454
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
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East Asian
type: Population
allele count: 1
allele frequency: 1.588057805304113e-4
allele num: 6297
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.833e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

QD
type: SiteQuality
SIO_000300: 2.353e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.207310612749426e-5
allele num: 45304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8037
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.655e0

DP
type: SiteQuality
SIO_000300: 1.411881e6

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 1.439e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.334e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6279
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9058
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4444
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.21483942414175e-5
allele num: 45150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
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DP
type: SiteQuality
SIO_000300: 1.401788e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.516e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.882e1

MQ
type: SiteQuality
SIO_000300: 5.875e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6199
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.244820077670775e-5
allele num: 44547
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
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allele num: 7870
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DP
type: SiteQuality
SIO_000300: 1.35629e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.122e1

VQSLOD
type: SiteQuality
SIO_000300: -2.568e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.253724279371662e-5
allele num: 44371
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6169
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4417
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South Asian
type: Population
allele count: 0
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DP
type: SiteQuality
SIO_000300: 1.347531e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

MQRankSum
type: SiteQuality
SIO_000300: -1.342e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.095e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.391e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

Other
type: Population
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Latino
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allele count: 0
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allele num: 9007
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 2.335084646818447e-4
allele num: 8565
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.289796666056054e-5
allele num: 43672
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 1.0865e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 1.328614e6

VQSLOD
type: SiteQuality
SIO_000300: -1.173e0

QD
type: SiteQuality
SIO_000300: 2.159e1

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6886
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
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African
type: Population
allele count: 1
allele frequency: 1.424095699230988e-4
allele num: 7022
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 567
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.690453766089497e-4
allele num: 41409
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.238e1

DP
type: SiteQuality
SIO_000300: 1.278797e6

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.756e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.379e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

South Asian
type: Population
allele count: 34
allele frequency: 4.886461626904283e-3
allele num: 6958
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 2.065e1

MQ
type: SiteQuality
SIO_000300: 6.083e1

DP
type: SiteQuality
SIO_000300: 1.331986e6

FS
type: SiteQuality
SIO_000300: 6.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7064
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.101722723543889e-4
allele num: 7314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.401367899029309e-5
allele num: 42547
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4261
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 571
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.063e1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.387162e6

QD
type: SiteQuality
SIO_000300: 2.0e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 519
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 8.917424647761727e-4
allele num: 5607
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.153045449860868e-5
allele num: 38812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5257
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4125
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e-1

FS
type: SiteQuality
SIO_000300: 1.003e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

DP
type: SiteQuality
SIO_000300: 1.492723e6

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 3.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

East Asian
type: Population
allele count: 3
allele frequency: 5.706676811869887e-4
allele num: 5257
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4125
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.30890052356021e-3
allele num: 6876
num of homozygotes: 0

South Asian
type: Population
allele count: 16
allele frequency: 2.853575887283753e-3
allele num: 5607
num of homozygotes: 0

Latino
type: Population
allele count: 90
allele frequency: 1.062072220911022e-2
allele num: 8474
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.926782273603083e-3
allele num: 519
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.44e0

FS
type: SiteQuality
SIO_000300: 1.003e0

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 1.492723e6

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38695
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4159
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8315
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5655
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 521
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5271
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.596e1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

DP
type: SiteQuality
SIO_000300: 1.4668e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8315
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4159
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6939
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 521
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5655
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38695
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.92e-1

QD
type: SiteQuality
SIO_000300: 1.596e1

FS
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 1.4668e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 547
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40811
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

DP
type: SiteQuality
SIO_000300: 1.464952e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.286e0

VQSLOD
type: SiteQuality
SIO_000300: -2.186e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

QD
type: SiteQuality
SIO_000300: 1.553e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.414e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 597
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6341
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.441976679622432e-5
allele num: 45025
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7771
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

QD
type: SiteQuality
SIO_000300: 1.856e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.492269e6

MQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.806e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.286835671084803e-4
allele num: 7771
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6341
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45025
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

VQSLOD
type: SiteQuality
SIO_000300: -7.806e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

DP
type: SiteQuality
SIO_000300: 1.492269e6

QD
type: SiteQuality
SIO_000300: 1.856e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9195
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6369
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 1.491e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

DP
type: SiteQuality
SIO_000300: 1.501547e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.406e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45487
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9206
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.120327700972862e-4
allele num: 7812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6423
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.8808e1

VQSLOD
type: SiteQuality
SIO_000300: -4.558e0

QD
type: SiteQuality
SIO_000300: 2.459e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.134e0

DP
type: SiteQuality
SIO_000300: 1.512832e6

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9261
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8445
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.256134153348514e-5
allele num: 46991
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.384642899725766e-4
allele num: 8387
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

DP
type: SiteQuality
SIO_000300: 1.5636e6

FS
type: SiteQuality
SIO_000300: 7.704e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.494e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

QD
type: SiteQuality
SIO_000300: 1.804e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9287
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.212389380530973e-4
allele num: 4520
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.857e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

DP
type: SiteQuality
SIO_000300: 1.588335e6

African
type: Population
allele count: 3
allele frequency: 3.528166529460191e-4
allele num: 8503
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.302925989672978e-4
allele num: 9296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 4.275378206533655e-3
allele num: 9122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 8.393486654356219e-4
allele num: 47656
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.422821760283061e-4
allele num: 4522
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.59957e6

QD
type: SiteQuality
SIO_000300: 1.741e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.724e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.877e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.672e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9147
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097799408420567e-5
allele num: 47669
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.02e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 1.596493e6

VQSLOD
type: SiteQuality
SIO_000300: -2.268e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 2.86e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

African
type: Population
allele count: 1
allele frequency: 1.175502527330434e-4
allele num: 8507
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.732e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

DP
type: SiteQuality
SIO_000300: 1.600597e6

QD
type: SiteQuality
SIO_000300: 2.636e1

VQSLOD
type: SiteQuality
SIO_000300: -2.862e0

MQ
type: SiteQuality
SIO_000300: 5.904e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.688e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.189446783552232e-5
allele num: 47739
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9413
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.45e-1

DP
type: SiteQuality
SIO_000300: 1.60539e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.81e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.924e1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.092575541977065e-5
allele num: 47788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 2.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 1.612983e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.041e0

FS
type: SiteQuality
SIO_000300: 7.672e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

African
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allele count: 0
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allele num: 8511
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.033805437816603e-4
allele num: 9673
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47780
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DP
type: SiteQuality
SIO_000300: 1.613384e6

VQSLOD
type: SiteQuality
SIO_000300: 3.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.896e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47783
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African
type: Population
allele count: 36
allele frequency: 4.229820232640112e-3
allele num: 8511
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
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MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.228e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

DP
type: SiteQuality
SIO_000300: 1.617321e6

QD
type: SiteQuality
SIO_000300: 1.533e1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.091875156890637e-5
allele num: 47804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9311
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.862e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

QD
type: SiteQuality
SIO_000300: 1.051e1

MQ
type: SiteQuality
SIO_000300: 5.892e1

DP
type: SiteQuality
SIO_000300: 1.618786e6

MQRankSum
type: SiteQuality
SIO_000300: -8.82e-1

FS
type: SiteQuality
SIO_000300: 4.069e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.166e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.09209397686144e-5
allele num: 47799
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.62048e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -2.715e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.82e-2

QD
type: SiteQuality
SIO_000300: 3.209e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47786
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.00250626566416e-4
allele num: 9975
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.621417e6

QD
type: SiteQuality
SIO_000300: 2.402e1

VQSLOD
type: SiteQuality
SIO_000300: 7.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.86e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.00070049034324e-4
allele num: 9993
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47775
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.622402e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.195e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

QD
type: SiteQuality
SIO_000300: 1.176e1

FS
type: SiteQuality
SIO_000300: 4.826e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093364036005861e-5
allele num: 47770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
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MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.622249e6

QD
type: SiteQuality
SIO_000300: 1.121e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.265e0

FS
type: SiteQuality
SIO_000300: 2.384e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.095425685728056e-5
allele num: 47723
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
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African
type: Population
allele count: 0
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allele num: 8509
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.681e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.152e0

QD
type: SiteQuality
SIO_000300: 9.58e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9289
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097095522701059e-5
allele num: 47685
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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allele num: 9950
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8507
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.618955e6

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.015e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

QD
type: SiteQuality
SIO_000300: 2.156e1

FS
type: SiteQuality
SIO_000300: 3.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.22e-1

African
type: Population
allele count: 1
allele frequency: 1.175502527330434e-4
allele num: 8507
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
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Other
type: Population
allele count: 0
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allele num: 629
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47673
num of homozygotes: 0

Latino
type: Population
allele count: 0
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allele num: 9285
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.008e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.918e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.619447e6

QD
type: SiteQuality
SIO_000300: 1.457e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

East Asian
type: Population
allele count: 0
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allele num: 6617
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47630
num of homozygotes: 0

Other
type: Population
allele count: 0
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African
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.396e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

DP
type: SiteQuality
SIO_000300: 1.624706e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

QD
type: SiteQuality
SIO_000300: 6.92e0

FS
type: SiteQuality
SIO_000300: 2.494e0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

Other
type: Population
allele count: 0
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allele num: 628
num of homozygotes: 0

Latino
type: Population
allele count: 0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4507
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.1000021000021e-5
allele num: 47619
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
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allele num: 6618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.99e-2

QD
type: SiteQuality
SIO_000300: 2.881e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 1.616876e6

FS
type: SiteQuality
SIO_000300: 0.0e0

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.110987668036885e-4
allele num: 9001
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44849
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4399
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South Asian
type: Population
allele count: 20
allele frequency: 2.477393781741608e-3
allele num: 8073
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.629e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.77e-2

DP
type: SiteQuality
SIO_000300: 1.464937e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.67e-1

QD
type: SiteQuality
SIO_000300: 2.144e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44157
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.12410071942446e-4
allele num: 8896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6331
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7761
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 3.19e1

VQSLOD
type: SiteQuality
SIO_000300: -1.798e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.427127e6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6281
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4335
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43674
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.646e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.401502e6

MQRankSum
type: SiteQuality
SIO_000300: -1.689e0

QD
type: SiteQuality
SIO_000300: 2.788e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.173e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 583
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7407
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43274
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.383011e6

QD
type: SiteQuality
SIO_000300: 1.341e1